Diastereoselective Tandem Michael−Intramolecular Wittig Reactions of a Cyclic Phosphonium Ylide with 8-Phenylmenthyl Enoates-Reference-Cited by-同舟云学术

Diastereoselective Tandem Michael−Intramolecular Wittig Reactions of a Cyclic Phosphonium Ylide with 8-Phenylmenthyl Enoates

Published:2001-01-17 Issue:3 Volume:66 Page:890-893
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Nagao Tomoko¹,Suenaga Takanori¹,Ichihashi Takao¹,Fujimoto Tetsuya¹,Yamamoto Iwao¹,Kakehi Akikazu¹,Iriye Ryozo¹

Affiliation:

1. Department of Functional Polymer Science, Shinshu University, Tokida Ueda 386-8567, Japan, Department of Chemistry and Material Engineering, Shinshu University, Wakasato Nagano 380-8553, Japan, and Department of Bioscience and Biotechnology, Shinshu University, Kami-Ina, Nagano 399-4598, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo001379a

Reference9 articles.

1. Ca11N6(CN2)2 and Ca4N2(CN2): The True Nature of an “Unusual Binary Nitride” Is Finally Revealed

2. Reaction of a Cyclic Phosphonium Ylide with α,β-Unsaturated Thioesters

3. Synthesis of Seven-Membered Cyclic Enol Ether Derivatives from the Reaction of a Cyclic Phosphonium Ylide with α,β-Unsaturated Esters

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