Arndt‐Eistert ‐Reaktionen in der Kohlenhydratchemie. — Synthesen biologisch wichtiger Kohlenhydrate, 10. 3‐Acetylamino‐2,3‐didesoxyheptosen aus Hept‐2‐enonsäureestern-Reference-Cited by-同舟云学术

Arndt‐Eistert ‐Reaktionen in der Kohlenhydratchemie. — Synthesen biologisch wichtiger Kohlenhydrate, 10. 3‐Acetylamino‐2,3‐didesoxyheptosen aus Hept‐2‐enonsäureestern

Published:1977-11 Issue:11 Volume:110 Page:3655-3663
ISSN:0009-2940
Container-title:Chemische Berichte
language:en
Short-container-title:Chem. Ber.

Author:

Dyong Ingolf¹,Hohenbrink Wilfried¹

Affiliation:

1. Organisch‐Chemisches Institut der Universität Münster, Orléans‐Ring 23, D‐4400 Münster

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19771101119

Reference32 articles.

1. Zur Synthese und 1 H‐NMR‐Spektroskopie von 2,3,6‐Tridesoxyhexosen und ihren O ‐Benzyl‐glycosiden

2. Arndt‐Eistert ‐Reaktionen in der Kohlenhydratchemie. – Synthesen biologisch wichtiger Kohlenhydrate, 2. Totalsynthese der Rhodinose

3. Synthesen biologisch wichtiger Kohlenhydrate, 3: Sehr einfache Synthese von DL ‐Amicetose

4. Synthese vonD-Forosamin, des 4-Dimethylamino-Zuckers aus Spiramycin

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1. Stereoselective synthesis of β-amino-γ-butyrolactones;Tetrahedron: Asymmetry;2002-09

2. Use of aldolases in the synthesis of non-carbohydrate natural products. Stereoselective synthesis of aspicilin C-3—C-9 fragment;Canadian Journal of Chemistry;1997-01-01

3. A New Synthesis ofN-Acetyl-4-Deoxy-D-Neuraminic Acid;Journal of Carbohydrate Chemistry;1991-01

4. Diastereoselective conjugate addition of ammonia in the synthesis of chiral pyrrolidines;Journal of the Chemical Society, Perkin Transactions 1;1990

5. Asymmetric Induction in the Intramolecular Conjugate Addition of g- or d-Carbamoyloxy-a,b-unsaturated Esters. A New Method for Diastereoselective Amination and Divergent Syntheases of 3-Amino-2,3,6-Trideoxyhexoses;HETEROCYCLES;1989