Lithium Enolates Derived from Pyroglutaminol: Mechanism and Stereoselectivity of an Azaaldol Addition-Reference-Cited by-同舟云学术

Lithium Enolates Derived from Pyroglutaminol: Mechanism and Stereoselectivity of an Azaaldol Addition

Published:2016-08-08 Issue:32 Volume:138 Page:10276-10283
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Houghton Michael J.¹,Huck Christopher J.¹,Wright Stephen W.²,Collum David B.¹

Affiliation:

1. Department of Chemistry and Chemical Biology Baker Laboratory, Cornell University Ithaca, New York 14853-1301, United States

2. Worldwide Medicinal Chemistry, Pfizer Global Research and Development, 445 Eastern Point Road, Groton, Connecticut 06340, United States

Funder

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.6b05481

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3. Pyroglutamic acid: a versatile building block in asymmetric synthesis

4. Lithium Enolates Derived from Pyroglutaminol: Aggregation, Solvation, and Atropisomerism

5. Stereoselective alkylations of a bicyclic lactam derived from pyroglutamic acid

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