Lithiated Oppolzer Enolates: Solution Structures, Mechanism of Alkylation, and Origin of Stereoselectivity-Reference-Cited by-同舟云学术

Lithiated Oppolzer Enolates: Solution Structures, Mechanism of Alkylation, and Origin of Stereoselectivity

Published:2022-12-19 Issue:51 Volume:144 Page:23379-23395
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Lui Nathan M.¹^ORCID,MacMillan Samantha N.¹^ORCID,Collum David B.¹^ORCID

Affiliation:

1. Department of Chemistry and Chemical Biology Baker Laboratory, Cornell University Ithaca, New York 14853-1301, 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.2c09341

Reference119 articles.

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3. Organolithium Reagents in Pharmaceutical Asymmetric Processes

4. Optimization of Organolithium Reactions

5. A survey of approximately 700 total syntheses compiled by H. J. Reich and co-workers revealed LDA to be the most commonly used reagent. The database currently resides at: The Hans Reich’s Collection. https://organicchemistrydata.org/hansreich/resources/syntheses/?index=groupby%2Finformation&page=acknowledgment%2F (accessed 2021-10-23).

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