Highly Enantioselective Intra- and Intermolecular [2 + 2] Photocycloaddition Reactions of 2-Quinolones Mediated by a Chiral Lactam Host: Host−Guest Interactions, Product Configuration, and the Origin of the Stereoselectivity in Solution-Reference-Cited by-同舟云学术

Highly Enantioselective Intra- and Intermolecular [2 + 2] Photocycloaddition Reactions of 2-Quinolones Mediated by a Chiral Lactam Host: Host−Guest Interactions, Product Configuration, and the Origin of the Stereoselectivity in Solution

Published:2002-06-14 Issue:27 Volume:124 Page:7982-7990
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Bach Thorsten¹,Bergmann Hermann¹,Grosch Benjamin¹,Harms Klaus¹

Affiliation:

1. Contribution from the Lehrstuhl für Organische Chemie I, Technische Universität München, D-85747 Garching, Germany and Fachbereich Chemie, Philipps-Universität Marburg, D-35032 Marburg, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0122288

Reference59 articles.

1. Catalytic Asymmetric Synthesis

2. High optical yields in a photochemical cycloaddition. Lack of cooperativity as a clue to mechanism

3. Asymmetrische Synthese bei Photo‐, Elektro‐ und Alkalimetall‐Pinakolisierungen von Benzaldehyd und Phenonen im chiralen Medium DDB

4. Chiral solvent-induced asymmetric synthesis. Part 2. Photosynthesis of optically enriched hexahelicenes

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