About: Highly selective enzymatic kinetic resolution of primary amines at 80 degrees C: a comparative study of carboxylic acids and their ethyl esters as acyl donors

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About: Highly selective enzymatic kinetic resolution of primary amines at 80 degrees C: a comparative study of carboxylic acids and their ethyl esters as acyl donors Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 2007 (uk) article scientifique publié en 2007 (fr) im August 2007 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q56950188-FF65EB41-3DBA-4A4E-896E-44E83C36A08D
publication date	2007-08-03 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56950188-84C34467-A3C5-4AF9-B625-FE1A3BF0C849
language of work or name	English
author name string	wds:Q56950188-174DF8F4-474B-4996-8347-8DB419109ACD wds:Q56950188-469B2BAE-B113-468D-821D-03D09F2E28E6 wds:Q56950188-9A66957B-5DE8-47DB-AD48-FCB098FB9BF5 wds:Q56950188-D23D7D41-F716-41CD-946A-60737B727EBA
author name string	Michèle Bertrand Malek Nechab Gérard Gil Nadia Azzi
rdfs:label	Highly selective enzymatic kinetic resolution of primary amines at 80 degrees C: a comparative study of carboxylic acids and their ethyl esters as acyl donors (en) Highly selective enzymatic kinetic resolution of primary amines at 80 degrees C: a comparative study of carboxylic acids and their ethyl esters as acyl donors (nl)
skos:prefLabel	Highly selective enzymatic kinetic resolution of primary amines at 80 degrees C: a comparative study of carboxylic acids and their ethyl esters as acyl donors (en) Highly selective enzymatic kinetic resolution of primary amines at 80 degrees C: a comparative study of carboxylic acids and their ethyl esters as acyl donors (nl)
name	Highly selective enzymatic kinetic resolution of primary amines at 80 degrees C: a comparative study of carboxylic acids and their ethyl esters as acyl donors (en) Highly selective enzymatic kinetic resolution of primary amines at 80 degrees C: a comparative study of carboxylic acids and their ethyl esters as acyl donors (nl)
author	wds:Q56950188-3777EF7B-CCAB-4CF0-B129-61BC298958BB wds:Q56950188-C4F67E88-BCE4-4E40-AADB-F28989E776D7
author	Nicolas Vanthuyne Stéphane Gastaldi
title	wds:Q56950188-5441A0A5-89C4-4481-9108-1D2E5923A855
title	Highly selective enzymatic kinetic resolution of primary amines at 80 degrees C: a comparative study of carboxylic acids and their ethyl esters as acyl donors (en)
page(s)	wds:Q56950188-026F32A4-630C-4979-8712-C697317220D8
page(s)	6918-6923
instance of	wds:Q56950188-70EA77DC-F17A-475D-B21B-B63EDA6F22CE
instance of	scholarly article
PubMed ID	wds:Q56950188-A123A62E-5B35-4BC4-9D80-4DC862A829C3
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17676806
PubMed ID	17676806
published in	wds:Q56950188-3CEE5CD6-F262-472E-A6B6-2F1F0FE72203
published in	Journal of Organic Chemistry
issue	wds:Q56950188-47534F37-3257-4CFC-B899-E67A18D4192E
volume	wds:Q56950188-C17345B1-44E7-40FF-A13B-289215B18C21
issue	18
volume	72
DOI	wds:Q56950188-3D7BFC41-D750-493F-8170-F59D3F3B3654
DOI	http://dx.doi.org/10.1021/JO071069T
DOI	10.1021/JO071069T
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56950188
is cites work of	Enantioselective syntheses of indanes: from organocatalysis to C-H functionalization Enzymatic enantiomeric resolution of phenylethylamines structurally related to amphetamine Enzymatic synthesis of N-Acylethanolamines: Direct method for the aminolysis of esters Enzymatic reactions and synthesis of n-butyl caproate: esterification, transesterification and aminolysis using a recombinant lipase from Geobacillus thermoleovorans CCR11.
is cites work of	wds:Q41455127-4B2C1E1F-ACB2-47A9-A9C8-4BDF65B0336E wds:Q38686285-6712397E-4104-4CE6-A4F9-250E20A336B0 wds:Q58814018-74F7BA40-3FAA-4304-85F9-ED726FCAB303 wds:Q42934286-AE3BEA30-5513-4EAB-A02B-8A698666E6BB

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