Controlling, Understanding, and Redirecting the Thermal Rearrangement of 3,3-Dicyano-1,5-enynes-Reference-Cited by-同舟云学术

Controlling, Understanding, and Redirecting the Thermal Rearrangement of 3,3-Dicyano-1,5-enynes

Published:2018-10-31 Issue:47 Volume:140 Page:16134-16139
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Scott Sarah K.¹,Sanders Jacob N.²,White Katherine E.¹,Yu Roland A.²,Houk K. N.²^ORCID,Grenning Alexander J.¹^ORCID

Affiliation:

1. Department of Chemistry, University of Florida, P.O. Box 117200, Gainesville, Florida 32611, United States

2. Department of Chemistry and Biochemistry, University of California—Los Angeles, 607 Charles E. Young Drive East, Box 951569, Los Angeles, California 90095-1569, United States

Funder

National Institute of General Medical Sciences

Department of Chemistry, University of Florida

College of Liberal Arts and Sciences, University of Florida

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.8b08553

Reference27 articles.

1. The formation of 5,6,7,8-Tetrahydronaphthalene-1,3-dicarbonitrile by thermal rearrangement of Cyclohex-1-enyl(prop-2-ynyl)malononitrile

2. 1256. Allenes. Part X. The Claisen–Cope rearrangement of propargyl vinyl systems

3. The Thermal Rearrangement of 1-Alken-5-yncs and 1,2,5-Alkatrienes1

4. Stereochemistry of the thermal acetylenic Cope rearrangement. Experimental test for a 1,4-cyclohexenediyl as a mechanistic intermediate

5. W(CO)5(L)-Catalyzed Formal Cope Rearrangement of Allenyl Silyl Enol Ethers

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