Stereodivergent Syntheses of Highly Substituted Enantiopure 4-Alkoxy-3,6-dihydro-2H-1,2-oxazines by Addition of Lithiated Alkoxyallenes to Carbohydrate-Derived Aldonitrones-Reference-Cited by-同舟云学术

Stereodivergent Syntheses of Highly Substituted Enantiopure 4-Alkoxy-3,6-dihydro-2H-1,2-oxazines by Addition of Lithiated Alkoxyallenes to Carbohydrate-Derived Aldonitrones

Published:2005-03 Issue:6 Volume:2005 Page:1003-1019
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Helms Matthias,Schade Wolfgang,Pulz Robert,Watanabe Toshiko,Al-Harrasi Ahmed,Fišera Lubor,Hlobilová Iva,Zahn Gernot,Reißig Hans-Ulrich

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference73 articles.

1. Stereoselective Homologation–Amination of Aldehydes by Addition of Their Nitrones to C-2 Metalated Thiazoles—A General Entry to α-Amino Aldehydes and Amino Sugars

2. Formylation of carbohydrates and the evolution of synthetic routes to artificial oligosaccharides and glycoconjugates

3. A convenient synthesis of iminosugar-C-glycosides via organometallic addition to N-benzyl-N-glycosylhydroxylamines

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