Diastereofacial selectivity in Diels-Alder cycloadditions involving vinyl sulfoxides-Reference-Cited by-同舟云学术

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Diastereofacial selectivity in Diels-Alder cycloadditions involving vinyl sulfoxides

Published:1986-01 Issue:50 Volume:27 Page:6041-6044
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kahn S.D,Hehre W.J

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. Chirality Transfer via Sigmatropic Rearrangements

2. S.D. Kahn and W.J. Hehre, J. Am. Chem. Soc., submitted.

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2. Sulfoxide-Induced Stereoselection in [1,5]-Sigmatropic Hydrogen Shifts of Vinylallenes. A Computational Study;The Journal of Organic Chemistry;2007-03-01

3. Influence of Diene Substitution on Diels−Alder Reactions between Vinyl Dihydronaphthalenes and (SS)-2-(p-Tolylsulfinyl)-1,4-benzoquinone;The Journal of Organic Chemistry;2003-04-22

4. Explorations in Organic Chemistry Leading to the Total Synthesis of (±)-Gelsemine;Journal of the American Chemical Society;2002-07-27

5. β-Trifluoroacetylvinyl phenyl sulfoxide—synthesis, Diels–Alder reaction and computational study;J. Chem. Soc., Perkin Trans. 1;2002

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