Asymmetrisch 1,6-induzierte Hetero-Diels-Alder-Reaktion chiraler Oxabutadiene zur De-novo-Synthese enantiomerenreiner Kohlenhydrate: Umkehr der Seitendifferenzierung durch Variation des Lewis-Säure-Initiators-Reference-Cited by-同舟云学术

Asymmetrisch 1,6-induzierte Hetero-Diels-Alder-Reaktion chiraler Oxabutadiene zur De-novo-Synthese enantiomerenreiner Kohlenhydrate: Umkehr der Seitendifferenzierung durch Variation des Lewis-Säure-Initiators

Published:1994-05-02 Issue:9 Volume:106 Page:1031-1032
ISSN:0044-8249
Container-title:Angewandte Chemie
language:de
Short-container-title:Angew. Chem.

Author:

Tietze Lutz F.,Schneider Christoph,Montenbruck Andrea

Publisher

Wiley

Subject

General Medicine

Reference54 articles.

1. Sequentielle Transformationen in der Organischen Chemie eine Synthesestrategie mit Zukunft

2. Sequential Transformations in Organic Chemistry: A Synthetic Strategy with a Future

3. (b) Comprehensive Organic Synthesis, Vol. 5, Pergamon Press, New York, 1991, S. 451;

4. Domino-reactions: The tandem-knoevenagel-hetero-diels-alder reaction and its application in natural product synthesis

5. (d) , Hetero-Diels-Alder-Methodology in Organic Synthesis, Academic Press, San Diego, CA, USA, 1987;

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