Enhanced Diastereoselectivity via Confinement: Diastereoselective Photoisomerization of 2,3-Diphenyl-1-benzoylcyclopropane Derivatives within Zeolites-Reference-Cited by-同舟云学术

Enhanced Diastereoselectivity via Confinement: Diastereoselective Photoisomerization of 2,3-Diphenyl-1-benzoylcyclopropane Derivatives within Zeolites

Published:2004-07-21 Issue:17 Volume:69 Page:5528-5536
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Sivaguru J.¹,Sunoj Raghavan. B.¹,Wada Takehiko¹,Origane Yumi¹,Inoue Yoshihisa¹,Ramamurthy V.¹

Affiliation:

1. Department of Chemistry, Tulane University, New Orleans, Louisiana 70118, Department of Chemistry, Indian Institute of Technology, Bombay, Mumbai 400076, India, Department of Molecular Chemistry and PRESTO (JST), Osaka University, 2-1 Yamada-oka, Suita 565-0871, Japan, and ICORP Entropy Control Project, JST, 4-6-3 Kamishinden, Toyonaka 560-0085, Japan.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo049697n

Reference31 articles.

1. Reactive-State Spin-Dependent Diastereoselective Photoisomerization of trans,trans-2,3-Diphenylcyclopropane-1- carboxylic Acid Derivatives Included in Zeolites

2. Introduction of the amide function into 1,3,2-dioxaphospholenes with pentavalent phosphorus

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