Variable Strategy toward Carbasugars and Relatives As Illustrated by Diastereoselective Synthesis of 1-Deoxy-1-amino-pseudo-β-d-gulopyranose (Alias 1,2,4-Tri-epi-validamine)-Reference-Cited by-同舟云学术

Variable Strategy toward Carbasugars and Relatives As Illustrated by Diastereoselective Synthesis of 1-Deoxy-1-amino-pseudo-β-d-gulopyranose (Alias 1,2,4-Tri-epi-validamine)

Published:1999-09-23 Issue:8 Volume:1 Page:1213-1215
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Rassu Gloria¹,Auzzas Luciana¹,Pinna Luigi¹,Zanardi Franca¹,Battistini Lucia¹,Casiraghi Giovanni¹

Affiliation:

1. Istituto per l'Applicazione delle Tecniche Chimiche Avanzate ai Problemi Agrobiologici, CNR, Via Vienna 2, I-07100 Sassari, Italy, and Dipartimento Farmaceutico, Università di Parma, Parco Area delle Scienze 27A, I-43100 Parma, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol990880q

Reference8 articles.

1. Compounds of Phosphorus and Fluorine. III. Preparation of Mono- and Diphosphonate Derivatives from Tetraethyl 3,3,4,4,5,5-Hexafluoro-1-cyclopenten-1,2-ylenediphosphonate1

2. Alicyclic carbohydrates. XXXIII. Epimerization of pseudo-.alpha.-DL-: talopyranose to pseudo-.alpha.-DL-galactopyranose. Proton magnetic resonance studies

3. Synthesis of 3-0-(p-tolylsulfonyl)-.beta.-D-altro-heptulopyranose and its conversion into 2,7:3,4-dianhydro-.beta.-D-allo-heptulopyranose

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