PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
29400958-0	2018	Spin-Center Shift-Enabled Direct Enantioselective alpha-Benzylation of Aldehydes with Alcohols.	Alcohols	86-94	spindlin 1	Homo sapiens	0-4	
29400958-1	2018	Nature routinely engages alcohols as leaving groups, as DNA biosynthesis relies on the removal of water from ribonucleoside diphosphates by a radical-mediated "spin-center shift" (SCS) mechanism.	Alcohols	25-33	spindlin 1	Homo sapiens	160-164	
29400958-3	2018	We report herein an enantioselective alpha-benzylation of aldehydes using alcohols as alkylating agents based on the mechanistic principle of spin-center shift.	Alcohols	74-82	spindlin 1	Homo sapiens	142-146	
24700693-2	2014	Alcohols are typically used to probe the reactive spin states of carbenes: O-H insertions are assumed to be characteristic of singlet states, whereas C-H insertions are typical for the triplets.	Alcohols	0-8	spindlin 1	Homo sapiens	50-54	
11084289-6	2000	In model experiments using Fe(3+)-catalyzed nucleophilic addition of methanol or tert-butanol to the respective spin trap the respective alkoxyl radical adducts were formed in aqueous solution as transient species in the presence of high concentrations of the alcohol.	Alcohols	260-267	spindlin 1	Homo sapiens	112-116