1,4-Addition of Lithium Diisopropylamide to Unsaturated Esters: Role of Rate-Limiting Deaggregation, Autocatalysis, Lithium Chloride Catalysis, and Other Mixed Aggregation Effects-Reference-Cited by-同舟云学术

1,4-Addition of Lithium Diisopropylamide to Unsaturated Esters: Role of Rate-Limiting Deaggregation, Autocatalysis, Lithium Chloride Catalysis, and Other Mixed Aggregation Effects

Published:2010-10-20 Issue:44 Volume:132 Page:15610-15623
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ma Yun¹,Hoepker Alexander C.¹,Gupta Lekha¹,Faggin Marc F.¹,Collum David B.¹

Affiliation:

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

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja105855v

Reference122 articles.

1. Deconjugative alkylation of the enolate anion derived from ethyl crotonate

2. Chiral Ligand-Controlled Asymmetric Conjugate Addition of Lithium Amides to Enoates

3. Stereoselective α-alkylation of α,β-unsaturated esters utilizing conjugate addition of nitrogen nucleophiles (R2NLi)

4. Asymmetric induction in the Michael Initiated Ring Closure reaction

5. The 2-Phenylselenenylation of 2-Enoic Esters

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