Chemo- and stereoselective functionalization of 7-oxabicyclo[2.2.1] hept-5-en-2-one derivatives with the system trichloroacetyl chloride/Zn(Cu)1
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Chemo- and stereoselective functionalization of 7-oxabicyclo[2.2.1]hept-5-en-2-one with dichloroketene
2. Regioselectivity of electrophilic additions to 7-oxabicyclo[2.2.1]heptenes controlled by remote substituents. Arenesulfonyl substituted 7-oxabicyclo[2.2.1]heptenes as stereo- and regioselective chiral dienophiles
3. The Preparation of Optically Pure 7-Oxabicyclo [2.2.1]hept-2-ene Derivatives. The CD Spectrum of (+)-(1R)-7-Oxabicyclo [2.2.1]hept-5-en-2-one
4. Optical resolution of 7-oxabicyclo[2.2.1]hept-21-ene derivatives. Diastereoselectivity in the formation of cyanohydrine-brucine complexes
5. Naked sugars as synthetic intermediates. Total synthesis of L-daunosamine
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1. Formation of β-Lactones by [2+2] Cycloaddition of Dichloroketene with Unreactive Carbonyl Compounds;Chemical Research in Chinese Universities;2018-09-14
2. The Staudinger reaction of imines derived from 7-oxanorbornenone: formation of spiranic oxazinone versus β-lactam rings;Tetrahedron Letters;2002-09
3. Resolution of 7-oxabicyclo[2.2.1]hept-5-en-2-one via cyclic aminals;Tetrahedron: Asymmetry;1999-02
4. Synthesis of β-lactones. Part 7.1 α-Chloro- and α,α-dichloro-β-lactones by aldolization of carbonyl compounds with lithium ester enolates derived from chlorinated phenyl alkanoates: an unusual course of the Darzens reaction;Journal of the Chemical Society, Perkin Transactions 1;1997
5. Using ring-opening reactions of oxabicyclic compounds as a strategy in organic synthesis;Topics in Current Chemistry;1997
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