Organocatalytic enantioselective Diels–Alder reaction between hydroxymaleimides and in situ generated nitrosoalkenes for direct preparation of chiral hemiketals with 1,2-oxazine skeleton-Reference-Cited by-同舟云学术

Organocatalytic enantioselective Diels–Alder reaction between hydroxymaleimides and in situ generated nitrosoalkenes for direct preparation of chiral hemiketals with 1,2-oxazine skeleton

Published:2021 Issue:22 Volume:8 Page:6215-6219
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Xiang Min¹²,Li Chen-Yi¹²,Zhang Jian¹²,Zou Ying¹²,Li Wen-Sheng¹²,Tian Fang¹,Wan Wen-Juan¹,Wang Li-Xin¹^ORCID

Affiliation:

1. Key Laboratory of Asymmetric Synthesis and Chirotechnology of Sichuan Province, Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu 610041, China

2. University of Chinese Academy of Sciences, Beijing 100049, China

Abstract

Organocatalytic Enantioselective IEDDA reaction between hydroxymaleimides and in situ generated nitrosoalkenes has been disclosed, a series of chiral hemiketals containing 5,6-dihydro-4H-l,2-oxazines and succinimide frameworks have been prepared.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO01022K

Reference38 articles.

1. Recent Advances in the Chemistry of Conjugated Nitrosoalkenes and Azoalkenes

2. Recent Contributions to Hetero Diels-Alder Reactions

3. Chemistry of Six-Membered Cyclic Oxime Ethers. Application in the Synthesis of Bioactive Compounds

4. β-Hydroxyimino Phosphorus Derivatives. An Efficient Tool in Organic Synthesis

5. The Nitrosocarbonyl Hetero-Diels-Alder Reaction as a Useful Tool for Organic Syntheses

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