reference/17402101

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17402101

Outgoing Links

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endingPage	54
issn	1477-0520 1477-0539
issueIdentifier	16
pageRange	5748-54
publicationName	Organic & Biomolecular Chemistry
startingPage	5748
bibliographicCitation	Zhang Q, Xiao X, Lin L, Liu X, Feng X. Highly enantioselective synthesis of γ-substituted butenolides via the vinylogous Mukaiyama-Michael reaction catalyzed by a chiral scandium(III)-N,N'-dioxide complex. Org Biomol Chem. 2011 Aug 21;9(16):5748–54. doi: 10.1039/c1ob05558e. PMID: 21717015.
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date	2011-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1039/c1ob05558e https://pubmed.ncbi.nlm.nih.gov/21717015
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Highly enantioselective synthesis of γ-substituted butenolides via the vinylogous Mukaiyama–Michael reaction catalyzed by a chiral scandium(iii)–N,N′-dioxide complex
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Total number of triples: 46.