Vicarious Silylative Mukaiyama Aldol Reaction: A Vinylogous Extension-Reference-Cited by-同舟云学术

Vicarious Silylative Mukaiyama Aldol Reaction: A Vinylogous Extension

Published:2008-06-13 Issue:14 Volume:73 Page:5446-5451
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Curti Claudio¹,Sartori Andrea¹,Battistini Lucia¹,Rassu Gloria¹,Burreddu Paola¹,Zanardi Franca¹,Casiraghi Giovanni¹

Affiliation:

1. Dipartimento Farmaceutico, Università di Parma, Viale G. P. Usberti 27A, I-43100 Parma, Italy, and Istituto di Chimica Biomolecolare del CNR, Traversa La Crucca 3, I-07040 Li Punti, Sassari, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo800741c

Reference34 articles.

1. Variable Strategy toward Carbasugars and Relatives. 1. Stereocontrolled Synthesis of Pseudo-β-d-gulopyranose, Pseudo-β-d-xylofuranose, (Pseudo-β-d-gulopyranosyl)amine, and (Pseudo-β-d-xylofuranosyl)amine

2. Variable Strategy toward Carbasugars and Relatives. 2.1 Diversity-Based Synthesis of β-d-Xylo, β-d-Ribo, β-l-Arabino, and β-l-Lyxo 4a-Carbafuranoses and (4a-Carbafuranosyl)thiols

3. Synthesis of a Small Repertoire of Non-Racemic 5a-Carbahexopyranoses and 1-Thio-5a-carbahexopyranoses

4. Variable Strategy toward Carbasugars and Relatives. 4.1 Viable Access to (4a-Carbapentofuranosyl)amines, (5a-Carbahexopyranosyl)amines, and Amino Acids Thereof

5. Variable Strategy toward Carbasugars and Relatives. 5.1 Focus on Preparation of Chiral Nonracemic Medium-Sized Carbocycles

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