Tandem Asymmetric Conjugate Addition/α-Alkylation Using (S,S)-(+)-Pseudoephedrine as Chiral Auxiliary-Reference-Cited by-同舟云学术

Tandem Asymmetric Conjugate Addition/α-Alkylation Using (S,S)-(+)-Pseudoephedrine as Chiral Auxiliary

Published:2006-05-16 Issue:12 Volume:8 Page:2535-2538
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Reyes Efraim¹,Vicario Jose L.¹,Carrillo Luisa¹,Badía Dolores¹,Iza Ainara¹,Uria Uxue¹

Affiliation:

1. Departamento de Química Orgánica II, Facultad de Ciencia y Tecnología, Universidad del País Vasco-Euskal Herriko Unibertsitatea, P.O. Box 644, E-48080 Bilbao, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol060720w

Reference14 articles.

1. Maximizing Synthetic Efficiency: Multi-Component Transformations Lead the Way

2. Rhodium-Catalyzed Asymmetric 1,4-Addition and Its Related Asymmetric Reactions

3. Catalytic Asymmetric Tandem Transformations Triggered by Conjugate Additions

4. A New Entry of Nucleophiles in Rhodium-Catalyzed Asymmetric 1,4-Addition Reactions: Addition of Organozinc Reagents for the Synthesis of 2-Aryl-4-piperidones

5. (S,S)-(+)-Pseudoephedrine as Chiral Auxiliary in Asymmetric Aza-Michael Reactions. Unexpected Selectivity Change when Manipulating the Structure of the Auxiliary

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