Changes of Stereoselectivity in Diels–Alder Reactions by Hydrophobic Solvent Effects and byβ-Cyclodextrin-Reference-Cited by-同舟云学术

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Changes of Stereoselectivity in Diels–Alder Reactions by Hydrophobic Solvent Effects and byβ-Cyclodextrin

Published:1987-09 Issue:9 Volume:26 Page:896-897
ISSN:0570-0833
Container-title:Angewandte Chemie International Edition in English
language:en
Short-container-title:Angew. Chem. Int. Ed. Engl.

Author:

Schneider Hans-Jörg,Sangwan Naresh K.

Publisher

Wiley

Subject

General Chemistry,Catalysis

Cited by 126 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

1. Synthesis of cyclodextrin dimers via Diels–Alder reaction;Synthetic Communications;2023-09-07

2. SUBSTITUENT EFFECT IN [2+4] DIELS–ALDER CYCLOADDITION REACTIONS OF ANTHRACENE WITH C2X2 (X = H, F, Cl, Me): A COMPUTATIONAL INVESTIGATION;Journal of Structural Chemistry;2021-10

3. Computational investigation of the substituent effect in the [2 + 4] Diels–Alder cycloaddition reactions of HSi ≡Si( para ‐C 6 H 4 X ) with benzene;Journal of the Chinese Chemical Society;2021-01-05

4. Computational Investigation into the Solvent Effect on the Diels-Alder Reaction of Isobenzofuran and Ethylene;CHEM METHODOL;2020

5. Cycloaddition reactions in water;Green Sustainable Process for Chemical and Environmental Engineering and Science;2020

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