Mechanism and Stereoselectivity of the Stepwise 1,3-Dipolar Cycloadditions between a Thiocarbonyl Ylide and Electron-Deficient Dipolarophiles: A Computational Investigation-Reference-Cited by-同舟云学术

Mechanism and Stereoselectivity of the Stepwise 1,3-Dipolar Cycloadditions between a Thiocarbonyl Ylide and Electron-Deficient Dipolarophiles: A Computational Investigation

Published:2010-12-01 Issue:50 Volume:132 Page:17921-17927
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Lan Yu¹,Houk K. N.¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569, United States

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja108432b

Reference99 articles.

1. 1,3-Dipolar Cycloadditions. Past and Future

2. Kinetics and Mechanism of 1,3-Dipolr Cycloadditions

3. Cycloadditions— Definition, Classification, and Characterization

4. The first two-step 1,3-dipolar cycloadditions: non-stereospecificity

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