A rearrangement of saccharin-derived cyclic ketimines with 3-chlorooxindoles leading to spiro-1,3-benzothiazine oxindoles-Reference-Cited by-同舟云学术

A rearrangement of saccharin-derived cyclic ketimines with 3-chlorooxindoles leading to spiro-1,3-benzothiazine oxindoles

Published:2021 Issue:86 Volume:57 Page:11322-11325
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Li Rui-Li¹,Fang Qing-Yun¹,Li Mei-Yuan¹,Wang Xiang-Shan¹,Zhao Li-Ming¹^ORCID

Affiliation:

1. School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, Jiangsu, China

Abstract

An unusual rearrangement of saccharin-derived cyclic ketimines (SDCIs) and 3-chlorooxindoles has been developed to provide a series of spiro-1,3-benzothiazine oxindoles.

Funder

Science and Technology Support Program of Jiangsu Province

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/2021/CC/D1CC04179G

Reference61 articles.

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4. Rh(III)‐Catalyzed Ring‐Opening Addition of Azabenzonorbornadienes with Cyclic N ‐Sulfonyl Ketimines via C−H Bond Activation

5. Iridium-catalyzed direct C–H arylation of cyclic N-sulfonyl ketimines with arylsiloxanes at ambient temperature

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