Tandem Addition/Cyclization Reaction of Organozinc Reagents to 2-Alkynyl Aldehydes: Highly Efficient Regio- and Enantioselective Synthesis of 1,3-Dihydroisobenzofurans and Tetrasubstituted Furans-Reference-Cited by-同舟云学术

Tandem Addition/Cyclization Reaction of Organozinc Reagents to 2-Alkynyl Aldehydes: Highly Efficient Regio- and Enantioselective Synthesis of 1,3-Dihydroisobenzofurans and Tetrasubstituted Furans

Published:2008-03-04 Issue:7 Volume:73 Page:2947-2950
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chai Zhuo¹,Xie Zheng-Feng¹,Liu Xin-Yuan¹,Zhao Gang¹,Wang Ji-De¹

Affiliation:

1. Laboratory of Modern Synthetic Organic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China, and Education Ministry Key Laboratory of Oil and Gas Fine Chemicals, XinJiang University, 14 Shengli Lu, Urumqi 830046, China zhaog@mail.sioc.ac.cn; awangjdl@xju.edu.cn

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo800029m

Reference16 articles.

1. Heterocycle synthesis by copper facilitated addition of heteroatoms to alkenes, alkynes and arenes

2. Versatile synthesis of (Z)-1-alkylidene-1,3-dihydroisobenzofurans and 1H-isochromenes by palladium-catalyzed cycloisomerization of 2-alkynylbenzyl alcohols

3. Gold-Catalyzed Benzylic CH Activation at Room Temperature

4. An Unusual Example of a 6-Endo-Dig Addition to an Unactivated Carbon-Carbon Triple Bond

5. Cyclization reactions of 2-alkynylbenzyl alcohol and 2-alkynylbenzylamine derivatives promoted by tetrabutylammonium fluoride

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