About: Enantioselective Synthesis of 4-Unsubstituted 3-Alkoxy- and 3-Aminoazetidin-2-ones from Formaldehyde N,N-Dialkylhydrazones We thank the Dirección General de Investigación Científica y Técnica for financial support (Grant no. PB 97/0747). We also tha

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About: Enantioselective Synthesis of 4-Unsubstituted 3-Alkoxy- and 3-Aminoazetidin-2-ones from Formaldehyde N,N-Dialkylhydrazones We thank the Dirección General de Investigación Científica y Técnica for financial support (Grant no. PB 97/0747). We also tha Goto Sponge NotDistinct Permalink

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scientific article published on 01 August 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 2000 (uk) im August 2000 veröffentlichter wissenschaftlicher Artikel (de) article scientifique publié en août 2000 (fr) artículu científicu espublizáu n'agostu de 2000 (ast) scientific article published on 01 August 2000 (en)
publication date	wds:Q73068269-9AD3AAAA-AC06-4378-A477-8637993644FD
publication date	2000-08-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q73068269-63DFD418-7367-4088-B961-0453B2301FB4
language of work or name	English
author name string	wds:Q73068269-84549F14-C997-4225-A9E4-193F0CA806D4 wds:Q73068269-DD673948-E299-42BB-8754-9CC433E71B30 wds:Q73068269-ED8CE010-38E9-4517-928F-05A001C01763
author name string	Monge A Ferrete A Llera JM
rdfs:label	Enantioselective Synthesis of 4-Unsubstituted 3-Alkoxy- and 3-Aminoazetidin-2-ones from Formaldehyde N,N-Dialkylhydrazones We thank the Dirección General de Investigación Científica y Técnica for financial support (Grant no. PB 97/0747). We also tha (en) Enantioselective Synthesis of 4-Unsubstituted 3-Alkoxy- and 3-Aminoazetidin-2-ones from Formaldehyde N,N-Dialkylhydrazones We thank the Dirección General de Investigación Científica y Técnica for financial support (Grant no. PB 97/0747). We also tha (nl)
skos:prefLabel	Enantioselective Synthesis of 4-Unsubstituted 3-Alkoxy- and 3-Aminoazetidin-2-ones from Formaldehyde N,N-Dialkylhydrazones We thank the Dirección General de Investigación Científica y Técnica for financial support (Grant no. PB 97/0747). We also tha (en) Enantioselective Synthesis of 4-Unsubstituted 3-Alkoxy- and 3-Aminoazetidin-2-ones from Formaldehyde N,N-Dialkylhydrazones We thank the Dirección General de Investigación Científica y Técnica for financial support (Grant no. PB 97/0747). We also tha (nl)
name	Enantioselective Synthesis of 4-Unsubstituted 3-Alkoxy- and 3-Aminoazetidin-2-ones from Formaldehyde N,N-Dialkylhydrazones We thank the Dirección General de Investigación Científica y Técnica for financial support (Grant no. PB 97/0747). We also tha (en) Enantioselective Synthesis of 4-Unsubstituted 3-Alkoxy- and 3-Aminoazetidin-2-ones from Formaldehyde N,N-Dialkylhydrazones We thank the Dirección General de Investigación Científica y Técnica for financial support (Grant no. PB 97/0747). We also tha (nl)
author	wds:Q73068269-12FE7B66-DF9F-419E-AE60-120B8C3324D5 wds:Q73068269-3D7111C2-7740-4F50-B83D-2EFD20F2F040
author	Rosario Fernández José María Lassaletta
title	wds:Q73068269-DB991FA2-12DA-4357-9DB5-0063817E8F6F
title	Enantioselective Synthesis of 4-Unsubstituted 3-Alkoxy- and 3-Aminoazetidin-2-ones from Formaldehyde N,N-Dialkylhydrazones We thank the Dirección General de Investigación Científica y Técnica for financial support (Grant no. PB 97/0747). We also thank the Ministerio de Educación y Ciencia for a doctoral fellowship to A.F. (en)
page(s)	wds:Q73068269-07DD3FBE-3D20-480E-9EF4-539151E14A01
page(s)	2893-2897
instance of	wds:Q73068269-0C772750-D1CB-412C-A0BD-40AAAF316426
instance of	scholarly article
main subject	wds:Q73068269-A4B25CA6-584D-496C-8B0F-384EBDC6F3A5
main subject	enantioselectivity
PubMed ID	wds:Q73068269-0F2A31D9-A664-43A6-B6A3-30CC414D0E6C
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11028001
PubMed ID	11028001
published in	wds:Q73068269-9CED0546-CC19-404C-9B10-7A9441E6A933
published in	Angewandte Chemie International Edition
issue	wds:Q73068269-08DD83E7-37CA-4E01-BF76-BADA38C4556C
volume	wds:Q73068269-F8EE5B91-E01E-415E-A420-90DEE1C9372C
issue	16
volume	39
DOI	wds:Q73068269-EFF1D0AB-E402-4AB2-9F48-48A4F55216BB
DOI	http://dx.doi.org/10.1002/1521-3773(20000818)39:16%3C2893::AID-ANIE2893%3E3.0.CO;2-E
DOI	10.1002/1521-3773(20000818)39:16<2893::AID-ANIE2893>3.0.CO;2-E
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73068269
is cites work of	Glyoxal bis-hydrazones: a new family of nitrogen ligands for asymmetric catalysis. Synthetic Approaches toward Monocyclic 3-Amino-β-lactams Stereoselective, Temperature-Dependent [2+2] Cycloaddition ofN,N-Dialkylhydrazones toN-Benzyl-N-(benzyloxycarbonyl)aminoketene
is cites work of	wds:Q30889928-C34D8A4A-C880-4B1F-BE26-78BDC95BBEDC wds:Q33809979-6330C22D-AE2D-4E9A-8AF8-C374A717A641 wds:Q59652209-3E8CE9A1-49D2-4398-BF5C-FA6C69D2035C

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