Diels-Alder reaction of (S)-2-p-tolylsulfinyl-2-cyclopentenone with Dane's diene: an efficient approach to the enantioselective preparation of perhydro-cyclopenta[a]phenanthrenes-Reference-Cited by-同舟云学术

Diels-Alder reaction of (S)-2-p-tolylsulfinyl-2-cyclopentenone with Dane's diene: an efficient approach to the enantioselective preparation of perhydro-cyclopenta[a]phenanthrenes

Published:1994-12 Issue:50 Volume:35 Page:9461-9464
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Alonso Inés,Carretero Juan C.,García Ruano José L.,Martín Cabrejas Luisa M.,López-Solera Isabel,Raithby Paul R.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. Asymmetric synthesis of carbon-carbon bonds using sulfinyl cycloalkenones, alkenolides, and pyrones

2. High .beta.-stereoselectivity in asymmetric radical addition to .alpha.-sulfinylcyclopentenones

3. Benzyl Methyl (S)-2-(p-Tolylsulfinyl)maleate, an Efficient Dienophile in Asymmetric Diels-Alder Reactions

4. Highly diastereoselective Diels-Alder reactions with (R)-ethoxy p-tolyl vinyl sulfonium tetrafluoroborate

5. Enantioselective synthesis of carbocyclic showdomycin derivative via asymmetric diels-alder reaction of (Ss)-3-(2-pyridylsulphinyl)acrylate

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