Steric and Conformational Control of the Regioselectivities in the Ene Reaction with Trisubstituted Cycloalkenes: Comparison of the Enophiles Singlet Oxygen, Triazolinedione, and Nitrosoarene-Reference-Cited by-同舟云学术

Steric and Conformational Control of the Regioselectivities in the Ene Reaction with Trisubstituted Cycloalkenes: Comparison of the Enophiles Singlet Oxygen, Triazolinedione, and Nitrosoarene

Published:2000-09-19 Issue:21 Volume:2 Page:3293-3296
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Adam Waldemar¹,Bottke Nils¹,Krebs Oliver¹

Affiliation:

1. Institut für Organische Chemie, Universität Würzburg, Am Hubland, D-97074 Würzburg, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol006475c

Reference23 articles.

1. Regioselectivity in the Ene Reaction of Singlet Oxygen with Alkenes

2. Stereochemical dependence of isotope effects in the ene reaction of N-phenyl-1,2,4-triazoline-3,5-dione with isomers of butene-d3

3. Mechanism of the ene reaction between singlet oxygen and olefins

4. Site specificity in the singlet oxygen-trisubstituted olefin reaction

5. Structural Studies of 1,8-Disubstituted Naphthalenes as Probes for nucleophile-electrophile interactions

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