PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
17828935-1	1988	Vibration-rotation lines of C(3) have been identified in the circumstellar spectrum of the obscured carbon star IRC+10216.	Carbon	100-106	complement C3	Homo sapiens	28-32	
2605680-5	1989	In this study, the logarithm of the isomerization rate to the delta 2 ester (log k12) correlated with the carbon-13 nuclear magnetic resonance chemical shift difference value at C-3 and C-4 of the delta 3 ester (delta delta (4-3)).	Carbon	106-112	complement C3	Homo sapiens	178-181	
17828935-3	1988	This high-resolution infrared detection of the pure carbon chain molecule C(3) allows the estimation of the equilibrium C-C bond length, 1.297 angstroms.	Carbon	52-58	complement C3	Homo sapiens	74-78	
17828935-3	1988	This high-resolution infrared detection of the pure carbon chain molecule C(3) allows the estimation of the equilibrium C-C bond length, 1.297 angstroms.	Carbon	120-121	complement C3	Homo sapiens	74-78	
3337720-3	1988	A non-cyclic pathway is suggested (reaction 2) for the direct biosynthesis of sucrose from the 3-PGA obtained from C-3, C-4 and C-5 of the six-carbon carboxylation adduct.	Carbon	143-149	complement C3	Homo sapiens	115-118	
3782058-5	1986	Furthermore, although the carbon-13 NMR signals of sphingosine C-1, C-2, C-3, C-4, and C-5 showed significant chemical shift differences between D-erythro and L-threo-sphingosines of lysosphingolipids, it was concluded that the signal position of sphingosine C-3 was the most important for the determination of D-erythro and L-threo configuration in the long chain base moieties of lysosphingolipids.	Carbon	26-32	complement C3	Homo sapiens	73-76	
3021640-4	1986	In the orthorhombic single crystal, we observed interaction of the unpaired electron, which is delocalized on the carbons C(3), C(4) and C(5) with one alpha-proton in position 4 and with four nonequivalent beta-protons connected with the carbon atoms C(2) and C(6).	Carbon	114-120	complement C3	Homo sapiens	122-126	
6852253-1	1983	The proton NMR analysis of D-glucosaminate dehydratase reaction in D2O revealed the incorporation of a deuterium atom at C-3 carbon of the product, 2-keto-3-deoxy-D-gluconate.	Carbon	125-131	complement C3	Homo sapiens	121-124	
2983185-5	1985	Calculated electron and spin densities indicate that the radical formed by H abstraction from the phenol oxygen does not remain localized on the oxygen, but is primarily a semiquinone aryl radical with significant unpaired spin density on the ring carbon atoms, particularly on C-3 and C-5.	Carbon	248-254	complement C3	Homo sapiens	278-281	
6375666-2	1984	Substitution of deuterium for hydrogen at the terminal carbon atoms (C-3) of Tris-BP significantly decreased both the mutagenic response and the formation rate of 2- bromoacrolein .	Carbon	55-61	complement C3	Homo sapiens	69-72	
6852253-3	1983	Thus, the dehydration of D-glucosaminate by the enzyme proceeds in a retention mode at C-3 carbon.	Carbon	91-97	complement C3	Homo sapiens	87-90	
4634828-4	1972	The carbon skeletons of formate and succinate were shown to arise from the C-2 and the C-3-C-6 atoms of the heterocyclic ring respectively by using N-methyl[2,3-(14)C(2)]isonicotinate.	Carbon	4-10	complement C3	Homo sapiens	87-90	
6119109-11	1981	The 13C incorporation data indicate that carbons 1, 2, 3, and 4, but not 5, of glutamate serve as the four-carbon donor for the carboxamide carbon, C-5, C-4, and C-3, respectively, of the pyrazole ring of pyrazofurin.	Carbon	41-48	complement C3	Homo sapiens	162-165	
6119109-11	1981	The 13C incorporation data indicate that carbons 1, 2, 3, and 4, but not 5, of glutamate serve as the four-carbon donor for the carboxamide carbon, C-5, C-4, and C-3, respectively, of the pyrazole ring of pyrazofurin.	Carbon	41-47	complement C3	Homo sapiens	162-165	
6119109-11	1981	The 13C incorporation data indicate that carbons 1, 2, 3, and 4, but not 5, of glutamate serve as the four-carbon donor for the carboxamide carbon, C-5, C-4, and C-3, respectively, of the pyrazole ring of pyrazofurin.	Carbon	107-113	complement C3	Homo sapiens	162-165	
728538-5	1978	Changes in carbon-13 chemical shifts fro ribose C-5" (downfield), C-2" C-3", and C-4" (upfield) and for adenine C-6 and C-8 (upfield) support this model.	Carbon	11-17	complement C3	Homo sapiens	71-74	
976263-3	1976	The alkylation of a histidine residue which is fast and extensive when the alkylation side chain is on the C-3 carbon atom, is dramatically decreased when alkylating side chain is shifted towards rings B and D. These results allow the location of this histidine in the vicinity of ring A and probably on the beta face of the steroid nucleus.	Carbon	111-117	complement C3	Homo sapiens	107-110	
29537039-3	2018	The obtained results complement not only existing ones, but for the first time the photoelectron spectra of C3, cyclic and linear C3H (c,l-C3H) as well as of the excited states of C3H3 are reported.	Carbon	21-22	complement C3	Homo sapiens	108-133	
33615793-2	2021	With the AAA approach introduced herein, challenging 3,3"-bisindolines bearing an all-carbon quaternary stereocenter (C3a) have been constructed in good yields with good to excellent enantioselectivties.	Carbon	86-92	complement C3	Homo sapiens	118-121	
31744771-3	2020	The accuracy of the calculated NMR chemical shift of the nominal but non-equivalent phenyl carbons C(3)/C(7) and C(4)/C(6) (ortho and meta to the acid -C(1)OOH group) of GA may not be evaluated using the experimental measurements at room temperature.	Carbon	84-98	complement C3	Homo sapiens	99-103	
31744771-5	2020	We further recognised that the C NMR chemical shifts of the nominal phenyl carbons (C(3)/C(7) and C(4)/C(6)) encode information for intramolecular hydrogen bonding network formed by GA conformers.	Carbon	68-82	complement C3	Homo sapiens	84-88	
33268656-3	2020	Extensive computational studies revealed that the driving force of the facile hydration of 9 is probably release of the ring strain of 9, which arises in part from the bent sp2-hybridized C3a carbon.	Carbon	192-198	complement C3	Homo sapiens	188-191	
34027944-2	2021	From an organic chemistry perspective, their rigid tricyclic molecular architectures with a fully substituted carbon center at the C3a-position pose a great challenge to synthetic chemists.	Carbon	110-116	complement C3	Homo sapiens	131-134	
33445177-3	2021	Stimulation with Poly I:C up-regulated C3aR mRNA and intra- and extracellular expression in NHEKs which showed functional relevance by up-regulating CXCL10 and down-regulating C3 expression in response to C3a.	Carbon	24-25	complement C3	Homo sapiens	39-42	
24168398-3	2013	The developed one-pot three-component consecutive reactions generate up to four contiguous stereocenters, including the C-3 all-carbon quaternary center, in a perfectly defined configuration.	Carbon	128-134	complement C3	Homo sapiens	120-123	
28102677-2	2017	The reaction proceeded via attack of the C-3 carbon of the indoles onto the C-2 position of the allylic moiety and intramolecular construction of the trifluoromethyl group by the intramolecular fluorine atom shift from the C-2 position to the C-3 position of the allyl unit.	Carbon	45-51	complement C3	Homo sapiens	41-44	
28102677-2	2017	The reaction proceeded via attack of the C-3 carbon of the indoles onto the C-2 position of the allylic moiety and intramolecular construction of the trifluoromethyl group by the intramolecular fluorine atom shift from the C-2 position to the C-3 position of the allyl unit.	Carbon	45-51	complement C3	Homo sapiens	243-246	
26340696-2	2015	The reaction afforded a variety of dimeric 2-oxindoles with a C-3/C-5" linkage having an all-carbon quaternary center at the pseudobenzylic position in high yields.	Carbon	93-99	complement C3	Homo sapiens	62-65	
29058431-3	2017	Photoextrusion of dinitrogen from these intermediates enables completely stereoselective formation of all C3a-C3a" and C3a-C7" carbon-carbon bonds and all the associated quaternary stereogenic centers.	Carbon	127-133	complement C3	Homo sapiens	106-109	
29058431-3	2017	Photoextrusion of dinitrogen from these intermediates enables completely stereoselective formation of all C3a-C3a" and C3a-C7" carbon-carbon bonds and all the associated quaternary stereogenic centers.	Carbon	134-140	complement C3	Homo sapiens	106-109	
26523465-1	2015	Substitution of the xanthene scaffold with bulky groups at C-3" and C-7" is expected to protect the electrophilic central methine carbon against nucleophilic attack and inhibit stacking.	Carbon	130-136	complement C3	Homo sapiens	59-62	
25429945-0	2014	Reaction of the C3(X(1)Sigmag (+)) carbon cluster with H2S(X(1)A1), hydrogen sulfide: photon-induced formation of C3S, tricarbon sulfur.	Carbon	35-41	complement C3	Homo sapiens	16-29	
23149626-1	2013	Carbon containing nano-sized molybdenum sulfide composites (MoS(x)C(y)) obtained by thermal decomposition reactions of (R(4)N)(2)MoS(4) (R = -H (C(0)), -CH(3) (C(1)), -C(3)H(7) (C(3)), and -C(6)H(13) (C(6))) show promising performance in visible-light driven photocatalytic hydrogen generation.	Carbon	0-6	complement C3	Homo sapiens	167-182	
24087851-3	2013	Moreover, the dimerization of tertiary bromide 6 efficiently establishes sterically hindered vicinal quaternary carbons (C3a and C3a"), which is a key linkage of intriguing bispyrrolo[2,3-b]indoline alkaloids, thereby enabling us to complete the total syntheses of racemic chimonanthine (9) and folicanthine (10).	Carbon	112-119	complement C3	Homo sapiens	121-124	
24087851-3	2013	Moreover, the dimerization of tertiary bromide 6 efficiently establishes sterically hindered vicinal quaternary carbons (C3a and C3a"), which is a key linkage of intriguing bispyrrolo[2,3-b]indoline alkaloids, thereby enabling us to complete the total syntheses of racemic chimonanthine (9) and folicanthine (10).	Carbon	112-119	complement C3	Homo sapiens	129-132	
23411433-2	2013	The studied transformation is based on the Mo(VI)-catalyzed isomerization of carbohydrate carbon skeleton and allows preparation of C-3 isomers of 3-C-branched aldoses in a simple way without formation of side products.	Carbon	90-96	complement C3	Homo sapiens	132-135	
23411433-3	2013	This rearrangement at C-3 carbon differs from the previously described epimerization at C-2 of aldoses catalyzed by Mo(VI) ions, known as Bilik reaction.	Carbon	26-32	complement C3	Homo sapiens	22-25	
23998190-2	2013	The NMR spectra show that the two delta-dicarbonyl sugars exist as two anomeric alpha- and beta-oxetanosyl forms, derived from the hemiacetalization of the C-3 hydroxyl group with the aldehydic carbon.	Carbon	42-48	complement C3	Homo sapiens	156-159	
20856944-0	2010	Facile nucleophilic substitution at the C3a tertiary carbon of the 3a-bromohexahydropyrrolo[2,3-b]indole scaffold.	Carbon	53-59	complement C3	Homo sapiens	40-43	
23199576-4	2013	Carbon isotopic data suggest a wide range of foraging strategies, characterized by mixed C(3)/C(4) to C(4)-dominated diets in wooded grasslands to open woodlands.	Carbon	0-6	complement C3	Homo sapiens	89-93	
21723185-4	2011	For second-period atoms bonded to C-3, two or more conformers are observed in CCl(4) solution, but when substitution by heavier atoms takes place, only one conformer is observed under the tested conditions, i.e., the gauche form with respect to the C=C-C-X dihedral angle.	Carbon	78-79	complement C3	Homo sapiens	34-37	
21723185-4	2011	For second-period atoms bonded to C-3, two or more conformers are observed in CCl(4) solution, but when substitution by heavier atoms takes place, only one conformer is observed under the tested conditions, i.e., the gauche form with respect to the C=C-C-X dihedral angle.	Carbon	78-79	complement C3	Homo sapiens	34-37	
21950073-4	2011	It this process, C-3 and C-4 atoms, which determine the "heavy" isotope composition of carbon of CO2 of the light-induced dark respiration component are split off from the hexose link of sucrose.	Carbon	87-93	complement C3	Homo sapiens	17-20	
21644568-2	2011	This method enables preparation of a variety of isoindolinones with substitution on the benzoyl fragment and C-3 carbon.	Carbon	113-119	complement C3	Homo sapiens	109-112	
21464327-4	2011	We present carbon isotope data from 452 fossil teeth that record differential rates of diet change from C(3) to mixed C(3)/C(4) or C(4) diets among East African herbivore families at seven different time periods during the Late Miocene to the Pliocene (9.9-3.2 Ma).	Carbon	11-17	complement C3	Homo sapiens	104-108	
21464327-4	2011	We present carbon isotope data from 452 fossil teeth that record differential rates of diet change from C(3) to mixed C(3)/C(4) or C(4) diets among East African herbivore families at seven different time periods during the Late Miocene to the Pliocene (9.9-3.2 Ma).	Carbon	11-17	complement C3	Homo sapiens	118-122	
20934908-4	2011	Also gamma-gauche and delta-effects of the alkyl groups at C-3 on the carbons of the aryl group at C-2 have been studied.	Carbon	70-77	complement C3	Homo sapiens	59-62	
21486309-2	2011	Plants using the C(4) pathway of carbon metabolism are marked by greater photosynthetic water and nitrogen-use efficiencies (PWUE and PNUE, respectively) than C(3) species, but it is unclear to what extent this is the case in C(3) -C(4) intermediate species.	Carbon	33-39	complement C3	Homo sapiens	159-163	
21486309-2	2011	Plants using the C(4) pathway of carbon metabolism are marked by greater photosynthetic water and nitrogen-use efficiencies (PWUE and PNUE, respectively) than C(3) species, but it is unclear to what extent this is the case in C(3) -C(4) intermediate species.	Carbon	33-39	complement C3	Homo sapiens	226-230	
21687356-11	2011	In(13) C- NMR spectra, C-3 and C-5 of the 1,2,4 - triazole nucleus were observed in the range of delta 147-166.9 ppm.	Carbon	7-8	complement C3	Homo sapiens	23-26	
19778056-6	2009	On the basis of the proposed mechanism, the glyoxal interaction with alanine through a decarboxylative aldol addition reaction can lead to the formation of 1,2-butanedione with the terminal ethyl carbon atoms originating from C-2" and C-3" atoms of alanine, and the similar interaction of 1,2-butanedione with a second molecule of alanine can lead to the formation of 3,4-hexanedione with both terminal ethyl carbon atoms originating from C-2" and C-3" atoms of alanine.	Carbon	196-202	complement C3	Homo sapiens	235-238	
19815185-1	2009	Reactions of amines and carbon nucleophiles with 4-sulfonyl-hex-3-enopyranoside generate a range of C-3 amino- and C-3 branched-chain sugars, which are analogues of 3-amino-3,6-dideoxy sugars and 3-C-branched-chain-3,6-dideoxy sugars.	Carbon	24-30	complement C3	Homo sapiens	100-118	
19778056-6	2009	On the basis of the proposed mechanism, the glyoxal interaction with alanine through a decarboxylative aldol addition reaction can lead to the formation of 1,2-butanedione with the terminal ethyl carbon atoms originating from C-2" and C-3" atoms of alanine, and the similar interaction of 1,2-butanedione with a second molecule of alanine can lead to the formation of 3,4-hexanedione with both terminal ethyl carbon atoms originating from C-2" and C-3" atoms of alanine.	Carbon	409-415	complement C3	Homo sapiens	235-238	
19778056-6	2009	On the basis of the proposed mechanism, the glyoxal interaction with alanine through a decarboxylative aldol addition reaction can lead to the formation of 1,2-butanedione with the terminal ethyl carbon atoms originating from C-2" and C-3" atoms of alanine, and the similar interaction of 1,2-butanedione with a second molecule of alanine can lead to the formation of 3,4-hexanedione with both terminal ethyl carbon atoms originating from C-2" and C-3" atoms of alanine.	Carbon	409-415	complement C3	Homo sapiens	448-451	
19778056-6	2009	On the basis of the proposed mechanism, the glyoxal interaction with alanine through a decarboxylative aldol addition reaction can lead to the formation of 1,2-butanedione with the terminal ethyl carbon atoms originating from C-2" and C-3" atoms of alanine, and the similar interaction of 1,2-butanedione with a second molecule of alanine can lead to the formation of 3,4-hexanedione with both terminal ethyl carbon atoms originating from C-2" and C-3" atoms of alanine.	Carbon	196-202	complement C3	Homo sapiens	448-451	
19437455-1	2009	In the acetylenic aldehyde oximes with substituents containing silicon and germanium, the (13)C NMR signal of the C-2 carbon of triple bond is shifted by 3.5 ppm to lower frequency and that of the C-3 carbon is moved by 7 ppm to higher frequency on going from E to Z isomer.	Carbon	118-124	complement C3	Homo sapiens	197-200	
19437455-1	2009	In the acetylenic aldehyde oximes with substituents containing silicon and germanium, the (13)C NMR signal of the C-2 carbon of triple bond is shifted by 3.5 ppm to lower frequency and that of the C-3 carbon is moved by 7 ppm to higher frequency on going from E to Z isomer.	Carbon	201-207	complement C3	Homo sapiens	197-200	
19437455-2	2009	A greater low-frequency effect of 5.5 ppm on the C-2 carbon signal and a greater high-frequency effect of 11 ppm on the C-3 carbon signal are observed in the analogous acetylenic ketone oximes.	Carbon	124-130	complement C3	Homo sapiens	120-123	
8030784-4	1994	However, if a double bond is present at the C-2 or C-3 carbon atoms, this cis=CH stretch absorption shows a hypsochromic shift to 3029-3028 and 3018-3017 cm-1, respectively.	Carbon	55-61	complement C3	Homo sapiens	51-54	
19078857-3	2008	The absolute configuration of the newly created chiral carbon center (C-3) was assigned by X-ray diffraction analysis of the intermediate 3(S)-isothiocyanato-D-glycero-D-galacto-decose 8a.	Carbon	55-61	complement C3	Homo sapiens	70-73	
18446757-5	2008	This indicated a shift from grass (C(4))- to tree (C(3))-derived carbon in the woodland, which was also supported by the two-phase (13)C enrichment with depth, i.e. C(3) vegetation dominated the top soil (0-10 cm), but the C(4) contribution increased with depth (more gradual).	Carbon	65-71	complement C3	Homo sapiens	51-55	
18446757-5	2008	This indicated a shift from grass (C(4))- to tree (C(3))-derived carbon in the woodland, which was also supported by the two-phase (13)C enrichment with depth, i.e. C(3) vegetation dominated the top soil (0-10 cm), but the C(4) contribution increased with depth (more gradual).	Carbon	65-71	complement C3	Homo sapiens	165-169	
17924615-2	2007	The structures of two representative nonpolar metabolites were identified earlier as dimers of 17beta-estradiol linked through a diaryl ether bond between the C-3 phenolic oxygen of one molecule and the C-2 or C-4 aromatic carbon of another.	Carbon	223-229	complement C3	Homo sapiens	159-162	
17321747-2	2007	The allylic alcohol portion comprising the C-3, C-4, and C-5 carbons is essential for this function.	Carbon	61-68	complement C3	Homo sapiens	43-46	
16358787-5	2005	As a result, atoms C-3 and C-4 of glucose become enriched with the heavy isotope, and subsequent mixing of atoms and the specificity of interactions in the photorespiration chain lead to an isotope weighting of the other atoms and an uneven distribution of carbon isotopes in glucose-6-phosphate and other photorespiration products.	Carbon	257-263	complement C3	Homo sapiens	19-22	
15680604-2	2005	The reactivity towards BCl(3) follows the order: C-4>or=C-2>C-6>C-3 for C-glucopyranosyl derivatives and C-3>or=C-4>C-6>C-2 for C-galactopyranosyl derivatives.	Carbon	24-25	complement C3	Homo sapiens	73-76	
15680604-2	2005	The reactivity towards BCl(3) follows the order: C-4>or=C-2>C-6>C-3 for C-glucopyranosyl derivatives and C-3>or=C-4>C-6>C-2 for C-galactopyranosyl derivatives.	Carbon	24-25	complement C3	Homo sapiens	114-117	
15624931-5	2005	The effect on enantioselectivity of the carbon chain length of the R group located (1) on the C-3 substituent of 4a-d, 6a-d, and 7a-d or (2) at C-5 in 8a-d and 9a-g was studied in detail.	Carbon	40-46	complement C3	Homo sapiens	94-97	
15255721-3	2004	Analysis of the (13)C NMR spectrum of the product mixture obtained from the photochemistry of the para isomer selectively deuterated at C3 and C5 (1d(2)()) revealed that the boron-substituted carbon is the active one in the phototransposition reactions in both acetonitrile and TFE.	Carbon	192-198	complement C3	Homo sapiens	136-145	
12739977-4	2003	The significance of the ligands is that by placing a ligating side chain on a ring carbon (C-3), rather than on a ring nitrogen, the ring nitrogen not bound to the metal and its attached proton are available for hydrogen bonding.	Carbon	83-89	complement C3	Homo sapiens	91-94	
12467423-6	2002	These compounds are reasonably formed by dehydration of unisolated intermediate products 7 and/or 8 obtained by coupling of two molecules through a linkage between the C-2 and the C-3" carbons.	Carbon	185-192	complement C3	Homo sapiens	180-183	
11966446-5	2002	beta-amino acids, with a specific side chain, can exist as the R or S isomers at either the alpha (C2) carbon or the beta (C3) carbon.	Carbon	127-133	complement C3	Homo sapiens	117-125	
11689080-3	2001	These azabicyclo[3.2.1] (bridged piperidine) series of compounds differ from the well-known benztropines by a 2-carbon spacer between C-3 and a diarylmethoxy moiety.	Carbon	112-118	complement C3	Homo sapiens	134-137	
11322734-5	2001	Reactivity of the polysaccharide C-atoms was determined by 13C NMR spectroscopy: For dextran this was C-3 > C-2 > C-4, while for pullulan it was C-6 > C-3 > C-2 > C-4.	Carbon	33-34	complement C3	Homo sapiens	102-105	
11322734-5	2001	Reactivity of the polysaccharide C-atoms was determined by 13C NMR spectroscopy: For dextran this was C-3 > C-2 > C-4, while for pullulan it was C-6 > C-3 > C-2 > C-4.	Carbon	33-34	complement C3	Homo sapiens	160-163	
10564066-6	1999	Compounds with 9-11 carbons at C-3 and 6-10 carbons at C-2 provided good separation (up to 2.7-fold) between activity and cytotoxicity.	Carbon	20-27	complement C3	Homo sapiens	31-34	
11674459-4	1999	On catalytic hydrogenation of the tetrachlorooxabicyclooctenones 3a-c hydrogenolysis of the exo-carbon-chlorine bonds occurs, leading to the endo-2,endo-4-dichloro-8-oxabicyclooctan-3-ones 8a-c. With lithium aluminum hydride and Grignard reagents, 8a and 3a form the endo-3-alcohols 12a-c and 13, respectively, the latter with uncertain configuration at C-3, in a highly stereoselective manner.	Carbon	96-102	complement C3	Homo sapiens	354-357	
8040062-0	1994	Synthesis and biological activities of C-3 heterocyclyl carbon-substituted new cephalosporins.	Carbon	56-62	complement C3	Homo sapiens	39-42	
18493652-2	2008	We synthesized palmitic acid with carbons C-3 through C-16 perdeuterated, C-1 and C-2 with 13C atoms and hydrogens at C-2.	Carbon	34-41	complement C3	Homo sapiens	42-45	
17580895-2	2007	The stereoelectronic properties of the substituents at the C-3 position and their interactions with the incoming carbon nucleophiles control the diastereoselectivity of addition at the C-5 position, favoring the formation of l-ido derivatives as major products in most of the cases studied.	Carbon	113-119	complement C3	Homo sapiens	59-62	
17445553-9	2007	Sparse sample algorithms used to estimate 12-hour AUC including C(0), C(1), C(2), C(3), C(4), and/or C(6) showed a good correlation with the calculated AUC(0-6) (r(2) = .81-.96).	Carbon	52-53	complement C3	Homo sapiens	82-86	
12227809-1	2002	Synthetic methodology that allows for incorporation of isotopic carbon at the C-3 and C-4 positions of bile salts is reported.	Carbon	64-70	complement C3	Homo sapiens	78-81	
12126417-4	2002	Protonation on nitrogen leads to nucleophilic attack at the C-3 carbon and yields C-3 products.	Carbon	64-70	complement C3	Homo sapiens	60-63	
12126417-4	2002	Protonation on nitrogen leads to nucleophilic attack at the C-3 carbon and yields C-3 products.	Carbon	64-70	complement C3	Homo sapiens	82-85	
11040520-0	2000	Spectroscopy of excited states of carbon anions above the photodetachment threshold Electronic transitions of C3- and C5- to states lying above the electron affinity of the neutral (EA) have been recorded in the gas phase by laser photodetachment spectroscopy.	Carbon	34-40	complement C3	Homo sapiens	110-120	
10420575-2	1999	Infrared and solid state NMR 13C analysis of MA and the ligand strongly suggests that antimony binds to N-methyl glucamine through the oxygen of C-3 carbon.	Carbon	149-155	complement C3	Homo sapiens	145-148