Acid-Catalyzed Rearrangement of 3-Aza-8-oxatricyclo[3.2.1. 02,4]octan-6-one Acetals. Highly Stereoselective Total Synthesis of 3-Amino-3-deoxy-D-altrose and Derivatives-Reference-Cited by-同舟云学术

Acid-Catalyzed Rearrangement of 3-Aza-8-oxatricyclo[3.2.1. 02,4]octan-6-one Acetals. Highly Stereoselective Total Synthesis of 3-Amino-3-deoxy-D-altrose and Derivatives

Published:1989-08-09 Issue:5 Volume:72 Page:882-891
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Nativi Cristina,Reymond Jean-Louis,Vogel Pierre

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference50 articles.

1. Synthesis of (?)-Conduritol C (1L-Cyclohex-5-ene-1,2,3/4-tetrol)

2. Highly Stereoselective Total Syntheses of 2,5-Anhydro-4-deoxy-D-ribo-hexonic Acid and of (1S)-1-C-(6-amino-7H-purin-8-yl)-1,4-anhydro-3-deoxy-D-erythro-pentitol (= cordycepin C)

3. Naked sugars as synthetic intermediates. Total synthesis of L-daunosamine

4. (b) in ?Trends in Synthetic Carbohydrate Chemistry?, Eds. D. Horton, L. D. Hawkins, and G. J. McGarvey, ACS Symp. Ser. 386, Washington, D. C., (1989), p. 197-241.

5. Stereoselective amino-hydroxylation of the double bond in 7-oxabicyclo[2.2.1]hept-5-en-2-yl derivatives. Remote substituent participation in acid-catalyzed decompositions of aziridines and triazolines

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