Formal Desymmetrization by a “Mitsunobu Trick” − Enantiomerically Purecis-3,4-DihydroxypyrrolineN-Oxides for the Enantiodivergent Synthesis of Trihydroxyindolizidines-Reference-Cited by-同舟云学术

Formal Desymmetrization by a “Mitsunobu Trick” − Enantiomerically Purecis-3,4-DihydroxypyrrolineN-Oxides for the Enantiodivergent Synthesis of Trihydroxyindolizidines

Published:1998-03 Issue:3 Volume:1998 Page:419-421
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Cicchi Stefano,Nunes José,Goti Andrea,Brandi Alberto

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/(SICI)1099-0690(199803)1998:3%3C419::AID-EJOC419%3E3.0.CO;2-V/fullpdf

Reference27 articles.

1. Assignment of the Absolute Configuration of Natural Lentiginosine by Synthesis and Enzymic Assays of Optically Pure (+) and (-)-Enantiomers

2. (1S,2S,7R,8aS)- and (1S,2S,7S,8aS)-trihydroxyoctahydroindolizine: Two new glycosidase inhibitors by nitrone cycloaddition strategy

3. Improved Syntheses of (+)-Lentiginosine and (1S,2S,7R,8aS)-Trihydroxyoctahydroindolizine by Butenol Cycloaddition to Enantiopure Protected Dihydroxy Pyrroline N-Oxides

4. Stereoselective Total Synthesis of (+)-Lentiginosine Using a Chiral Nitrone Intermediate

5. A Five-Membered Enantiopure Cyclic Nitrone from Malic Acid by Regioselective Oxidation of Cyclic Hydroxylamine. Synthesis of (1S,7S,8aR)-Octahydro-1,7-dihydroxyindolizine

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