Vinyl Carbocations Generated under Basic Conditions and Their Intramolecular C–H Insertion Reactions-Reference-Cited by-同舟云学术

Vinyl Carbocations Generated under Basic Conditions and Their Intramolecular C–H Insertion Reactions

Published:2019-05-13 Issue:23 Volume:141 Page:9140-9144
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wigman Benjamin¹,Popov Stasik¹,Bagdasarian Alex L.¹,Shao Brian¹,Benton Tyler R.¹,Williams Chloé G.¹,Fisher Steven P.²,Lavallo Vincent²^ORCID,Houk K. N.¹^ORCID,Nelson Hosea M.¹^ORCID

Affiliation:

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

2. Department of Chemistry, University of California, Riverside, California 92521, United States

Funder

Division of Chemistry

University of California, Los Angeles

Division of Graduate Education

Alfred P. Sloan Foundation

David and Lucile Packard Foundation

Pew Charitable Trusts

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.9b02110

Reference31 articles.

1. 100 Years of Carbocations and Their Significance in Chemistry1

2. Contemporary Carbocation Chemistry: Applications in Organic Synthesis

3. Conclusion of the classical-nonclassical ion controversy based on the structural study of the 2-norbornyl cation

4. Ueber die basischen Eigenschaften des Kohlenstoffs und die Constitution des sogenannten Triphenylmethyls

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