Quinine-Promoted, Enantioselective Boron-Tethered Diels–Alder Reaction by Anomeric Control of Transition-State Conformation-Reference-Cited by-同舟云学术

Quinine-Promoted, Enantioselective Boron-Tethered Diels–Alder Reaction by Anomeric Control of Transition-State Conformation

Published:2018-05-01 Issue:10 Volume:83 Page:5756-5765
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Scholl Katie¹,Dillashaw John¹,Timpy Evan¹,Lam Yu-hong²,DeRatt Lindsey¹,Benton Tyler R.¹,Powell Jacqueline P.¹,Houk K. N.²^ORCID,Morgan Jeremy B.¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, University of North Carolina Wilmington, Dobo Hall, Wilmington, North Carolina 28403, United States

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

Funder

University of North Carolina Wilmington

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b00938

Reference28 articles.

1. Recent Advances in Natural Product Synthesis by Using Intramolecular Diels−Alder Reactions

2. Recent applications of intramolecular Diels–Alder reactions to natural product synthesis

3. Alkenylboronate Tethered Intramolecular Diels−Alder Reactions

4. Diels–Alder reactions of dienylboron compounds with unactivated dienophiles: an application of boron tethering for substituted cyclohexenol synthesis

5. The temporary silicon connection in the control of the regiochemistry of 4 + 2 cycloadditions

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