Asymmetric Carbon−Carbon Bond Formations by Conjugate Additions of Lithiated N-Boc Allylic Amines to Nitroalkenes: Enantioselective Synthesis of Functionalized Cyclopentanoids-Reference-Cited by-同舟云学术

Asymmetric Carbon−Carbon Bond Formations by Conjugate Additions of Lithiated N-Boc Allylic Amines to Nitroalkenes: Enantioselective Synthesis of Functionalized Cyclopentanoids

Published:2002-06-29 Issue:16 Volume:4 Page:2747-2749
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Johnson Timothy A.¹,Curtis Michael D.¹,Beak Peter¹

Affiliation:

1. Department of Chemistry, Roger Adams Laboratory, University of Illinois at Urbana−Champaign, Urbana, Illinois 61801

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol026277g

Reference10 articles.

1. Anionic approaches to the construction of cyclopentanoids

2. Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. Asymmetric Synthesis of Highly Functionalized Aminocyclopentanes Using the Bridged Mode (β-Tether) Process

3. Alkylation of enolate ions generated regiospecifically via organocopper reactions. Synthesis of decalin sesquiterpene valerane and of prostaglandin model systems

4. Highly Diastereoselective and Enantioselective Carbon−Carbon Bond Formations in Conjugate Additions of Lithiated N-Boc Allylamines to Nitroalkenes: Enantioselective Synthesis of 3,4- and 3,4,5-Substituted Piperidines Including (−)-Paroxetine

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