A New 1-Alkoxy-2-(chalcogeno)allylic or 1-Alkoxy-2,4-bis(chalcogeno)penta-2,4-dienyl Cation: Highly-Regioselective Allylating or Penta-2,4-dienylating Electrophiles and Their Reactions-Reference-Cited by-同舟云学术

A New 1-Alkoxy-2-(chalcogeno)allylic or 1-Alkoxy-2,4-bis(chalcogeno)penta-2,4-dienyl Cation: Highly-Regioselective Allylating or Penta-2,4-dienylating Electrophiles and Their Reactions

Published:1998-08-28 Issue:19 Volume:63 Page:6619-6624
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yoshimatsu Mitsuhiro¹,Gotoh Satoshi¹,Ikeda Kazunari¹,Komori Motonori¹

Affiliation:

1. Department of Chemistry, Faculty of Education, Gifu University, Yanagido, Gifu 501-11, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9807767

Reference23 articles.

1. Syntheses of Seven- and Five-Membered Rings from Allyl Cations

2. Organic syntheses via the polybromo ketone-iron carbonyl reaction

3. Alkene synthesis via .beta.-functionalized organosilicon compounds

4. Chemistry of allene oxides

5. Highly Regio- and Stereoselective [3+2] Cyclopentanone Annulation Using a 3-(Alkylthio)-2-siloxyallyl Cationic Species

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