Unusual Temperature-Dependent Diastereoselectivity in the [2+2] Photocycloaddition (Paternò−Büchi Reaction) of Benzophenone to cis- and trans-Cyclooctene through Conformational Control-Reference-Cited by-同舟云学术

Unusual Temperature-Dependent Diastereoselectivity in the [2+2] Photocycloaddition (Paternò−Büchi Reaction) of Benzophenone to cis- and trans-Cyclooctene through Conformational Control

Published:2001-02-16 Issue:10 Volume:123 Page:2452-2453
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Adam Waldemar¹,Stegmann Veit R.¹,Weinkötz Stephan¹

Affiliation:

1. Institute of Organic Chemistry, University of Würzburg Am Hubland, D-97074 Würzburg, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja005744r

Reference31 articles.

1. (a) Griesbeck, A. G.; Fiege, M. InMolecular and SupramolecularPhotochemistry; Ramamurthy, V., Schanze, K. S., Eds.; Marcel Dekker: New York, 2000; Vol. 6, p 33.

2. Hydroxy-Directed Regio- and Diastereoselective [2+2] Photocycloaddition (Paternò−Büchi Reaction) of Benzophenone to Chiral Allylic Alcohols

3. Organic Photochemical Reactions. XIV. The Photocycloaddition of Acetone to Cyclooctene and 1,3-Cyclooctadiene

4. Divergent stereoselectivity in the photoaddition of alkanals and medium ring cycloalkenes

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