Regioselectivity Control in the Oxidative Formal [3 + 2] Annulations of Ketoxime Acetates and Tetrohydroisoquinolines-Reference-Cited by-同舟云学术

Regioselectivity Control in the Oxidative Formal [3 + 2] Annulations of Ketoxime Acetates and Tetrohydroisoquinolines

Published:2019-10-03 Issue:20 Volume:21 Page:8239-8243
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Qu Zhonghua¹,Zhang Feng¹²,Deng Guo-Jun¹^ORCID,Huang Huawen¹^ORCID

Affiliation:

1. Key Laboratory for Green Organic Synthesis and Application of Hunan Province, Key Laboratory of Environmentally Friendly Chemistry and Application of Ministry of Education, College of Chemistry, Xiangtan University, Xiangtan 411105, China

2. College of Science, Hunan Agricultural University, Changsha 410128, China

Funder

National Natural Science Foundation of China

Hunan Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02978

Reference47 articles.

1. Rearrangement of N-Oxyenamines and Related Reactions

2. Transition metal-catalyzed C–H functionalization of N-oxyenamine internal oxidants

3. O-Acyl oximes: versatile building blocks for N-heterocycle formation in recent transition metal catalysis

4. Metal-Involving Synthesis and Reactions of Oximes

5. α-Diazo oxime ethers for N-heterocycle synthesis

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