Catalyst-controlled diastereoselectivity reversal in the formation of dihydropyrans-Reference-Cited by-同舟云学术

Catalyst-controlled diastereoselectivity reversal in the formation of dihydropyrans

Published:2018 Issue:28 Volume:54 Page:3496-3499
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Kano Taichi¹²³⁴⁵^ORCID,Maruyama Hiroki¹²³⁴⁵,Homma Chihiro¹²³⁴⁵,Maruoka Keiji¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry

2. Graduate School of Science

3. Kyoto University

4. Sakyo

5. Kyoto 606-8502

Abstract

In dihydropyran synthesis, use of (S)-3b is crucial for overcoming the inherent trans-selectivity and obtaining unusual cis-adducts with high enantioselectivity.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CC/C8CC01443D

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5. Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels–Alder Reaction

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