Asymmetric 1,6-Induction in Hetero-Diels–Alder Reactions of Chiral Oxabutadienes for a De Novo Synthesis of Enantiomerically Pure Carbohydrates: Lewis Acid Dependent Reversal of Facial Selectivity-Reference-Cited by-同舟云学术

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Asymmetric 1,6-Induction in Hetero-Diels–Alder Reactions of Chiral Oxabutadienes for a De Novo Synthesis of Enantiomerically Pure Carbohydrates: Lewis Acid Dependent Reversal of Facial Selectivity

Published:1994-05-18 Issue:9 Volume:33 Page:980-982
ISSN:0570-0833
Container-title:Angewandte Chemie International Edition in English
language:en
Short-container-title:Angew. Chem. Int. Ed. Engl.

Author:

Tietze Lutz F.,Schneider Christoph,Montenbruck Andrea

Publisher

Wiley

Subject

General Chemistry,Catalysis

Cited by 64 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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3. De Novo Synthesis of Mono- and Oligosaccharides via Dihydropyran Intermediates;Chemistry - An Asian Journal;2017-04-20

4. Diastereoselective Diels–Alder Reactions of 1,7,9-Decatrien-3-ones to Highly Substituted Octalin Derivatives;Synthesis;2016-09-27

5. Glycochemical Applications of Diels-Alder Reaction;Current Organic Chemistry;2016-08-17

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