PMID-sentid Pub_year Sent_text comp_official_name comp_offset protein_name organism prot_offset 22260520-4 2012 Thus, a metalloenzyme-inspired polymeric imidazole Pd catalyst (MEPI-Pd) was readily prepared by the coordinative convolution of (NH(4))(2)PdCl(4) and poly[(N-vinylimidazole)-co-(N-isopropylacrylamide)(5)] in a methanol-water solution at 80 C for 30 min. imidazole 41-50 serpin family I member 2 Homo sapiens 64-68 22260520-4 2012 Thus, a metalloenzyme-inspired polymeric imidazole Pd catalyst (MEPI-Pd) was readily prepared by the coordinative convolution of (NH(4))(2)PdCl(4) and poly[(N-vinylimidazole)-co-(N-isopropylacrylamide)(5)] in a methanol-water solution at 80 C for 30 min. Palladium 51-53 serpin family I member 2 Homo sapiens 64-68 22260520-4 2012 Thus, a metalloenzyme-inspired polymeric imidazole Pd catalyst (MEPI-Pd) was readily prepared by the coordinative convolution of (NH(4))(2)PdCl(4) and poly[(N-vinylimidazole)-co-(N-isopropylacrylamide)(5)] in a methanol-water solution at 80 C for 30 min. Palladium 69-71 serpin family I member 2 Homo sapiens 64-68 22260520-4 2012 Thus, a metalloenzyme-inspired polymeric imidazole Pd catalyst (MEPI-Pd) was readily prepared by the coordinative convolution of (NH(4))(2)PdCl(4) and poly[(N-vinylimidazole)-co-(N-isopropylacrylamide)(5)] in a methanol-water solution at 80 C for 30 min. (nh(4))( 129-137 serpin family I member 2 Homo sapiens 64-68 22260520-4 2012 Thus, a metalloenzyme-inspired polymeric imidazole Pd catalyst (MEPI-Pd) was readily prepared by the coordinative convolution of (NH(4))(2)PdCl(4) and poly[(N-vinylimidazole)-co-(N-isopropylacrylamide)(5)] in a methanol-water solution at 80 C for 30 min. 5-(2'-naphthyl)-7-4-chlorophenyl-(2,3,6,8-tetrahydro)pyrrolo-(3,4-e)(1,4)-diazepine-6-thioxo-8-(1H,7H)one 139-143 serpin family I member 2 Homo sapiens 64-68 22260520-4 2012 Thus, a metalloenzyme-inspired polymeric imidazole Pd catalyst (MEPI-Pd) was readily prepared by the coordinative convolution of (NH(4))(2)PdCl(4) and poly[(N-vinylimidazole)-co-(N-isopropylacrylamide)(5)] in a methanol-water solution at 80 C for 30 min. poly[(n-vinylimidazole)-co-(n-isopropylacrylamide) 151-201 serpin family I member 2 Homo sapiens 64-68 22260520-4 2012 Thus, a metalloenzyme-inspired polymeric imidazole Pd catalyst (MEPI-Pd) was readily prepared by the coordinative convolution of (NH(4))(2)PdCl(4) and poly[(N-vinylimidazole)-co-(N-isopropylacrylamide)(5)] in a methanol-water solution at 80 C for 30 min. Methanol 211-219 serpin family I member 2 Homo sapiens 64-68 22260520-4 2012 Thus, a metalloenzyme-inspired polymeric imidazole Pd catalyst (MEPI-Pd) was readily prepared by the coordinative convolution of (NH(4))(2)PdCl(4) and poly[(N-vinylimidazole)-co-(N-isopropylacrylamide)(5)] in a methanol-water solution at 80 C for 30 min. Water 220-225 serpin family I member 2 Homo sapiens 64-68 22260520-6 2012 TEM observation and XPS and EDX analyses indicated that PdCl(2) and Pd(0) nanoparticles were uniformly dispersed in MEPI-Pd. palladium chloride 56-63 serpin family I member 2 Homo sapiens 116-120 22260520-6 2012 TEM observation and XPS and EDX analyses indicated that PdCl(2) and Pd(0) nanoparticles were uniformly dispersed in MEPI-Pd. pd(0) 68-73 serpin family I member 2 Homo sapiens 116-120 22260520-6 2012 TEM observation and XPS and EDX analyses indicated that PdCl(2) and Pd(0) nanoparticles were uniformly dispersed in MEPI-Pd. Palladium 56-58 serpin family I member 2 Homo sapiens 116-120 22260520-7 2012 MEPI-Pd was utilized for the allylic arylation/alkenylation/vinylation of allylic esters and carbonates with aryl/alkenylboronic acids, vinylboronic acid esters, and tetraaryl borates. Palladium 5-7 serpin family I member 2 Homo sapiens 0-4 22260520-7 2012 MEPI-Pd was utilized for the allylic arylation/alkenylation/vinylation of allylic esters and carbonates with aryl/alkenylboronic acids, vinylboronic acid esters, and tetraaryl borates. Esters 82-88 serpin family I member 2 Homo sapiens 0-4 22260520-7 2012 MEPI-Pd was utilized for the allylic arylation/alkenylation/vinylation of allylic esters and carbonates with aryl/alkenylboronic acids, vinylboronic acid esters, and tetraaryl borates. Carbonates 93-103 serpin family I member 2 Homo sapiens 0-4 22260520-7 2012 MEPI-Pd was utilized for the allylic arylation/alkenylation/vinylation of allylic esters and carbonates with aryl/alkenylboronic acids, vinylboronic acid esters, and tetraaryl borates. aryl/alkenylboronic acids 109-134 serpin family I member 2 Homo sapiens 0-4 22260520-7 2012 MEPI-Pd was utilized for the allylic arylation/alkenylation/vinylation of allylic esters and carbonates with aryl/alkenylboronic acids, vinylboronic acid esters, and tetraaryl borates. vinylboronic acid esters 136-160 serpin family I member 2 Homo sapiens 0-4 22260520-7 2012 MEPI-Pd was utilized for the allylic arylation/alkenylation/vinylation of allylic esters and carbonates with aryl/alkenylboronic acids, vinylboronic acid esters, and tetraaryl borates. tetraaryl borates 166-183 serpin family I member 2 Homo sapiens 0-4 22260520-8 2012 Even 0.8-40 mol ppm Pd of MEPI-Pd efficiently promoted allylic arylation/alkenylation/vinylation in alcohol and/or water with a catalytic turnover number (TON) of 20,000-1,250,000. Alcohols 100-107 serpin family I member 2 Homo sapiens 26-30 22260520-8 2012 Even 0.8-40 mol ppm Pd of MEPI-Pd efficiently promoted allylic arylation/alkenylation/vinylation in alcohol and/or water with a catalytic turnover number (TON) of 20,000-1,250,000. Water 115-120 serpin family I member 2 Homo sapiens 26-30 22260520-9 2012 Furthermore, MEPI-Pd efficiently promoted the Suzuki-Miyaura reaction of a variety of inactivated aryl chlorides as well as aryl bromides and iodides in water with a TON of up to 3,570,000. aryl chlorides 98-112 serpin family I member 2 Homo sapiens 13-17 22260520-9 2012 Furthermore, MEPI-Pd efficiently promoted the Suzuki-Miyaura reaction of a variety of inactivated aryl chlorides as well as aryl bromides and iodides in water with a TON of up to 3,570,000. aryl bromides 124-137 serpin family I member 2 Homo sapiens 13-17 22260520-9 2012 Furthermore, MEPI-Pd efficiently promoted the Suzuki-Miyaura reaction of a variety of inactivated aryl chlorides as well as aryl bromides and iodides in water with a TON of up to 3,570,000. Iodides 142-149 serpin family I member 2 Homo sapiens 13-17 22260520-9 2012 Furthermore, MEPI-Pd efficiently promoted the Suzuki-Miyaura reaction of a variety of inactivated aryl chlorides as well as aryl bromides and iodides in water with a TON of up to 3,570,000. Water 153-158 serpin family I member 2 Homo sapiens 13-17 22260520-10 2012 MEPI-Pd was reused for the allylic arylation and Suzuki-Miyaura reaction of an aryl chloride without loss of catalytic activity. aryl chloride 79-92 serpin family I member 2 Homo sapiens 0-4 22110064-11 2012 CONCLUSIONS: The novel association of SERPINI2 with refractive error and myopia is suggestive of a possible link between physiological pathways controlling eye growth and development and those controlling glucose metabolism. Glucose 205-212 serpin family I member 2 Homo sapiens 38-46 20018339-6 2010 (S)-Methyl-[16O,17O,18O]-phosphate (MePi*), 7 and enantiomeric [16O,17O,18O]-thiophosphate (TPi*), 10, were previously reported to exhibit weak electronic circular dichroism (ECD), although with 10 the result was considered to be uncertain. (s)-methyl-[16o,17o,18o]-phosphate 0-34 serpin family I member 2 Homo sapiens 36-40 20018339-6 2010 (S)-Methyl-[16O,17O,18O]-phosphate (MePi*), 7 and enantiomeric [16O,17O,18O]-thiophosphate (TPi*), 10, were previously reported to exhibit weak electronic circular dichroism (ECD), although with 10 the result was considered to be uncertain. 16o,17o,18o]-thiophosphate 64-90 serpin family I member 2 Homo sapiens 36-40 33790688-1 2019 Isoprene was efficiently converted to 1,6-dimethyl-1,5-cyclooctadiene (DMCOD) by selective [4+4]-cycloaddition with a catalyst formed by in situ reduction of [(MePI)FeCl(mu-Cl)]2 (MePI = [2-(2,6-(CH3)2-C6H3-N=C(CH3))-C4H5N]). isoprene 0-8 serpin family I member 2 Homo sapiens 160-164 33790688-1 2019 Isoprene was efficiently converted to 1,6-dimethyl-1,5-cyclooctadiene (DMCOD) by selective [4+4]-cycloaddition with a catalyst formed by in situ reduction of [(MePI)FeCl(mu-Cl)]2 (MePI = [2-(2,6-(CH3)2-C6H3-N=C(CH3))-C4H5N]). isoprene 0-8 serpin family I member 2 Homo sapiens 180-184 33790688-1 2019 Isoprene was efficiently converted to 1,6-dimethyl-1,5-cyclooctadiene (DMCOD) by selective [4+4]-cycloaddition with a catalyst formed by in situ reduction of [(MePI)FeCl(mu-Cl)]2 (MePI = [2-(2,6-(CH3)2-C6H3-N=C(CH3))-C4H5N]). 1,6-Dimethyl-1,5-cyclooctadiene 38-69 serpin family I member 2 Homo sapiens 160-164 33790688-1 2019 Isoprene was efficiently converted to 1,6-dimethyl-1,5-cyclooctadiene (DMCOD) by selective [4+4]-cycloaddition with a catalyst formed by in situ reduction of [(MePI)FeCl(mu-Cl)]2 (MePI = [2-(2,6-(CH3)2-C6H3-N=C(CH3))-C4H5N]). 1,6-Dimethyl-1,5-cyclooctadiene 38-69 serpin family I member 2 Homo sapiens 180-184 33790688-1 2019 Isoprene was efficiently converted to 1,6-dimethyl-1,5-cyclooctadiene (DMCOD) by selective [4+4]-cycloaddition with a catalyst formed by in situ reduction of [(MePI)FeCl(mu-Cl)]2 (MePI = [2-(2,6-(CH3)2-C6H3-N=C(CH3))-C4H5N]). dmcod 71-76 serpin family I member 2 Homo sapiens 160-164 33790688-1 2019 Isoprene was efficiently converted to 1,6-dimethyl-1,5-cyclooctadiene (DMCOD) by selective [4+4]-cycloaddition with a catalyst formed by in situ reduction of [(MePI)FeCl(mu-Cl)]2 (MePI = [2-(2,6-(CH3)2-C6H3-N=C(CH3))-C4H5N]). dmcod 71-76 serpin family I member 2 Homo sapiens 180-184 33790688-1 2019 Isoprene was efficiently converted to 1,6-dimethyl-1,5-cyclooctadiene (DMCOD) by selective [4+4]-cycloaddition with a catalyst formed by in situ reduction of [(MePI)FeCl(mu-Cl)]2 (MePI = [2-(2,6-(CH3)2-C6H3-N=C(CH3))-C4H5N]). 2-(2,6-(ch3)2-c6h3 188-206 serpin family I member 2 Homo sapiens 160-164 33790688-1 2019 Isoprene was efficiently converted to 1,6-dimethyl-1,5-cyclooctadiene (DMCOD) by selective [4+4]-cycloaddition with a catalyst formed by in situ reduction of [(MePI)FeCl(mu-Cl)]2 (MePI = [2-(2,6-(CH3)2-C6H3-N=C(CH3))-C4H5N]). c(ch3))-c4h5n 209-222 serpin family I member 2 Homo sapiens 160-164