About: Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds

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About: Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds Goto Sponge NotDistinct Permalink

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scientific article published on January 2008

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2008 (ast) наукова стаття, опублікована в січні 2008 (uk) scientific article published on January 2008 (en) مقالة علمية نشرت في يناير 2008 (ar)
publication date	wds:Q37464343-A6BF736E-244B-4F99-AD51-796D90B90926
publication date	2008-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37464343-0CC5A5E5-E9C0-4C17-87BE-1D956E3CBC9A
language of work or name	English
cites work	wds:Q37464343-0CEEFA9A-FE60-4060-BBAD-4C7D71B38754 wds:Q37464343-4D932EA2-679C-4BCD-B7FA-4C5719E61AAE wds:Q37464343-81730496-9F43-4472-8699-2959B678E7CC wds:Q37464343-89CFBA63-B8EE-4E10-A08A-7BDD73174C98 wds:Q37464343-BDE0077C-1A86-41C6-AF30-7A5E0787E113 wds:Q37464343-D50404C7-215A-45D7-BC18-D66CA05FB995 wds:Q37464343-DB902C3A-34E1-489B-AC5B-E865BDA1DB02 wds:Q37464343-E4FA01BB-639A-429E-AE7A-F6D015E7A36F wds:Q37464343-EDBBD05D-F43A-41FF-BA58-978610B62070 wds:Q37464343-FDBC68CA-A32C-4E4B-86CE-C82F9DA023F1
cites work	Nucleophilic Chiral Amines as Catalysts in Asymmetric Synthesis Enantioselective Staudinger synthesis of beta-lactams catalyzed by a planar-chiral nucleophile Catalytic asymmetric Staudinger reactions to form beta-lactams: an unanticipated dependence of diastereoselectivity on the choice of the nitrogen substituent Asymmetric catalysis with "planar-chiral" derivatives of 4-(dimethylamino)pyridine Catalytic asymmetric synthesis of piperidine derivatives through the [4 + 2] annulation of imines with allenes Synthesis of functionalized cyclopentenes through catalytic asymmetric [3+2] cycloadditions of allenes with enones. Recent approaches towards the asymmetric synthesis of alpha,alpha-disubstituted alpha-amino acids Asymmetric synthesis of highly substituted beta-lactones by nucleophile-catalyzed [2+2] cycloadditions of disubstituted ketenes with aldehydes Catalytic asymmetric synthesis of tertiary alkyl chlorides Enantioselective synthesis of protected amines by the catalytic asymmetric addition of hydrazoic acid to ketenes
author name string	wds:Q37464343-33E1917B-9ED9-4994-92FF-612AD964E46D wds:Q37464343-CC715F86-0FF9-41C9-9997-6A63AD461FD0
author name string	Gregory C Fu Jacob M Berlin
rdfs:label	Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds (en) Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds (nl) Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds (ast)
skos:prefLabel	Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds (en) Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds (nl) Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds (ast)
name	Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds (en) Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds (nl) Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds (ast)
title	wds:Q37464343-4E4A013E-5429-4659-A521-6C2D2ADBEF51
title	Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds (en)
page(s)	wds:Q37464343-CB8F112D-AF98-4CFA-948D-FA87DED4447A
page(s)	7048-7050
instance of	wds:Q37464343-26625515-D4B5-489E-8B6E-81DFAD180DD5
instance of	scholarly article
main subject	wds:Q37464343-17A5BE6C-0EA7-428E-8526-5158E83D8848 wds:Q37464343-2D158DDF-8C5B-48E9-857A-B4803A135408
main subject	cycloaddition enantioselectivity
PubMed ID	wds:Q37464343-9FC6F0ED-88EC-4A50-AF08-634DE9716B7D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18668500
PubMed ID	18668500
published in	wds:Q37464343-02288620-5CE8-451A-9328-21C9C6DCFFE3
published in	Angewandte Chemie International Edition
issue	wds:Q37464343-ACE6F2CE-4E85-4D84-96AC-1015EECC9AAA
volume	wds:Q37464343-AE3FA760-BB7B-45DD-BB9B-17904AEA28D3
issue	37
volume	47
DOI	wds:Q37464343-D27D060D-8640-4A68-BC46-873DD6466CFC
DOI	http://dx.doi.org/10.1002/ANIE.200802439
DOI	10.1002/ANIE.200802439
ResearchGate publication ID	wds:Q37464343-F7F1E866-7096-4E67-A2DA-E19C7E84F231
ResearchGate publication ID	23138856
PMCID	wds:Q37464343-4DCCA1B8-1673-490E-91D8-CCF225F33DE6
PMCID	2790040
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37464343
is cites work of	Academic cross-fertilization by public screening yields a remarkable class of protein phosphatase methylesterase-1 inhibitors Remodeling natural products: chemistry and serine hydrolase activity of a rocaglate-derived β-lactone The pharmacological landscape and therapeutic potential of serine hydrolases Synthesis of β-lactams by transition metal promoted Staudinger reactions: alternative synthetic approaches from transition metal enhanced organocatalysis to in situ, highly reactive intermediate synthesis and catalytic tandem reactions Discovery and optimization of sulfonyl acrylonitriles as selective, covalent inhibitors of protein phosphatase methylesterase-1. Competitive activity-based protein profiling identifies aza-β-lactams as a versatile chemotype for serine hydrolase inhibition BINEPINES: chiral binaphthalene-core monophosphepine ligands for multipurpose asymmetric catalysis Chemical probes and drug leads from advances in synthetic planning and methodology. Catalytic, asymmetric reactions of ketenes and ketene enolates. Tertiary amine-catalyzed and direct synthesis of α-chloroalkanesulfonylhydrazines from azodicarboxylates and sulfonyl chlorides. A ferrocenyl kaleidoscope: slow interconversion of six diastereo-atropisomers of 2,6-di-tert-butyl-9,10-diferrocenyltriptycene Catalytic asymmetric cycloaddition of ketenes and nitroso compounds: enantioselective synthesis of alpha-hydroxycarboxylic acid derivatives
is cites work of	wds:Q37689578-25F665C0-9BF0-49C4-9655-7E9124DA1D6F wds:Q50853979-F3A8E1A8-BDF9-4E2E-8771-BCAACBD3ACB0 wds:Q33360050-60A70715-0BD1-4B5B-88CA-E039CAD97AD1 wds:Q33890959-953C247C-BCB8-404C-9A67-73F8B46E0346 wds:Q26995817-641F646B-AED2-4EA8-9A3C-AD69A1118A9F wds:Q35129344-330105CA-4BB0-4C32-AA2B-AF54ED444B60 wds:Q35889116-7686B6FD-8831-4832-8777-B654714D7B3B

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