Enantioselective Diels−Alder Cycloadditions with (SS)-2-(p-Tolylsulfinyl)-1,4-naphthoquinone: Efficient Kinetic Resolution of Chiral Racemic Vinylcyclohexenes-Reference-Cited by-同舟云学术

Enantioselective Diels−Alder Cycloadditions with (SS)-2-(p-Tolylsulfinyl)-1,4-naphthoquinone: Efficient Kinetic Resolution of Chiral Racemic Vinylcyclohexenes

Published:1998-10-16 Issue:23 Volume:63 Page:8320-8330
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Carreño M. Carmen¹,Urbano Antonio¹,Di Vitta Claudio¹

Affiliation:

1. Departamento de Química Orgánica (C-I), Universidad Autónoma, Cantoblanco, 28049-Madrid, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9811874

Reference53 articles.

1. (b) Trost, B. M., Fleming, I., Paquette, L. A., Eds.Comprehensive OrganicSynthesis; Pergamon Press: Oxford, U.K., 1991; Vol. 5, Chapter 4.

2. .pi.-Facial selectivities in cycloadditions to norbornyl- and norbornenyl-fused p-benzoquinones

3. π-Facial stereoselectivity in the Diels–Alder reactions of a rigid carbocyclic diene: spiro(bicyclo[2.2.1]heptane-2,1′-[2,4]cyclopentadiene)

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