Ylide Hydrolysis in Tandem Reactions: A Highly Z/E-Selective Access to 3-Alkylidene Dihydrobenzofurans and Related Analogues-Reference-Cited by-同舟云学术

Ylide Hydrolysis in Tandem Reactions: A Highly Z/E-Selective Access to 3-Alkylidene Dihydrobenzofurans and Related Analogues

Published:2013-06-04 Issue:12 Volume:15 Page:3054-3057
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhu Jian-Bo¹,Wang Peng¹,Liao Saihu¹,Tang Yong¹

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, P. R. China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol401240z

Reference30 articles.

1. Phosphorus Ylides

2. The alkaline hydrolysis of sterically crowded phosphonium salts

3. Mechanism of hydrolysis of phosphonium salts and ylides

4. A General Method of Alkylation and Alkenylation Heterocycles

5. Synthesis of 3,11-dimethyl-2-nonacosanone, a sex pheromone of the German cockroach

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