Catalytic, Asymmetric Hypervinylogous Mukaiyama Aldol Reactions of Extended Furan-Based Silyl Enolates-Reference-Cited by-同舟云学术

Catalytic, Asymmetric Hypervinylogous Mukaiyama Aldol Reactions of Extended Furan-Based Silyl Enolates

Published:2011-08-11 Issue:17 Volume:13 Page:4738-4741
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Curti Claudio¹,Battistini Lucia¹,Sartori Andrea¹,Lodola Alessio¹,Mor Marco¹,Rassu Gloria¹,Pelosi Giorgio¹,Zanardi Franca¹,Casiraghi Giovanni¹

Affiliation:

1. Dipartimento Farmaceutico, Università degli Studi di Parma, Parco Area delle Scienze 27A, I-43124 Parma, Italy, Istituto di Chimica Biomolecolare del CNR, Traversa La Crucca 3, I-07100 Li Punti, Sassari, Italy, and Dipartimento di Chimica Generale ed Inorganica, Chimica Analitica, Chimica Fisica, Università degli Studi di Parma, Parco Area delle Scienze 17A, I-43124 Parma, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol2020626

Reference22 articles.

1. The Principle of Vinylogy.

2. The Application of the Principle of Vinylogy to Unsaturated Ketones

3. Modern Aldol Methods for the Total Synthesis of Polyketides

4. The Vinylogous Aldol Reaction: A Valuable, Yet Understated Carbon−Carbon Bond-Forming Maneuver

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