Diastereofacial selectivity in Diels-Alder cycloadditions of methyl acrylate to facially differentiated unsymmetrical Cyclohexa-1,3-dienes-Reference-Cited by-同舟云学术

Diastereofacial selectivity in Diels-Alder cycloadditions of methyl acrylate to facially differentiated unsymmetrical Cyclohexa-1,3-dienes

Published:1994-01 Issue:45 Volume:50 Page:13037-13048
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Coxon James M.,Tai Fong Siew,Lundie Karen,Quentin McDonald D.,Steel Peter J.,Marchand Alan P.,Zaragoza Florencio,Zope Umesh R.,Rajagopal D.,Bott Simon G.,Watson William H.,Kashyap Ram P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference20 articles.

1. .pi.-Facial selectivity in Diels-Alder reactions of hexacyclo[10.2.1.02,11.04,9.04,14.09,13]pentadeca-5,7-diene-3,10-dione

2. Facial differentiation in Diels-Alder reactions to dissymmetric cyclohexa-1,3-dienes

3. ⊼-Facial Stereoselectivity in Diels-Alder Reaction of Hexacyclo [7.4.2.01,9.03,7.04,14.06,15] Pentadecane-10,12-diene-2,8-dione

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3. A DFT investigation of Diels-Alder reaction of ethyl propiolate to the cage-annulated hexacyclo[7.5.2.01,6.06,13.08,12.010,14]hexadeca-2,4-diene-7,16-dione;Journal of the Serbian Chemical Society;2018

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