Facile Synthesis of Spiro[cyclohexane-1,3’-indoline]-2,2’-diones

Spiro[cyclohexane-1,3’-indoline]-2,2’-diones were easily prepared in good to high yields by the oxidation of N-aryl-N-methyl-2-oxocyclohexane-1-carboxamides in one pot with a short reaction time. The spiroindolinediones could be important for the total synthesis of natural products.

Bibliographic Details
Main Authors:	Katayama Shin-taro, Nishino Hiroshi
Format:	Article
Language:	English
Published:	De Gruyter 2019-12-01
Series:	Heterocyclic Communications
Subjects:	spiro[cyclohexane-1,3’-indoline]-2,2’-diones oxidative cyclization 5-exo cyclization radicals heterocycles
Online Access:	https://doi.org/10.1515/hc-2019-0022

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spelling	doaj-11409697166749d8899082a4160df4ee2021-09-06T19:19:48ZengDe GruyterHeterocyclic Communications2191-01972019-12-0125115716110.1515/hc-2019-0022Facile Synthesis of Spiro[cyclohexane-1,3’-indoline]-2,2’-dionesKatayama Shin-taro0Nishino Hiroshi1Department of Chemistry, Graduate School of Science, Kumamoto University, Kurokami 2-39-1, Chûou-Ku, Kumamoto 860-8555, JapanDepartment of Chemistry, Graduate School of Science, Kumamoto University, Kurokami 2-39-1, Chûou-Ku, Kumamoto 860-8555, JapanSpiro[cyclohexane-1,3’-indoline]-2,2’-diones were easily prepared in good to high yields by the oxidation of N-aryl-N-methyl-2-oxocyclohexane-1-carboxamides in one pot with a short reaction time. The spiroindolinediones could be important for the total synthesis of natural products.https://doi.org/10.1515/hc-2019-0022spiro[cyclohexane-1,3’-indoline]-2,2’-dionesoxidative cyclization5-exo cyclizationradicalsheterocycles
collection	DOAJ
language	English
format	Article
sources	DOAJ
author	Katayama Shin-taro Nishino Hiroshi
spellingShingle	Katayama Shin-taro Nishino Hiroshi Facile Synthesis of Spiro[cyclohexane-1,3’-indoline]-2,2’-diones Heterocyclic Communications spiro[cyclohexane-1,3’-indoline]-2,2’-diones oxidative cyclization 5-exo cyclization radicals heterocycles
author_facet	Katayama Shin-taro Nishino Hiroshi
author_sort	Katayama Shin-taro
title	Facile Synthesis of Spiro[cyclohexane-1,3’-indoline]-2,2’-diones
title_short	Facile Synthesis of Spiro[cyclohexane-1,3’-indoline]-2,2’-diones
title_full	Facile Synthesis of Spiro[cyclohexane-1,3’-indoline]-2,2’-diones
title_fullStr	Facile Synthesis of Spiro[cyclohexane-1,3’-indoline]-2,2’-diones
title_full_unstemmed	Facile Synthesis of Spiro[cyclohexane-1,3’-indoline]-2,2’-diones
title_sort	facile synthesis of spiro[cyclohexane-1,3’-indoline]-2,2’-diones
publisher	De Gruyter
series	Heterocyclic Communications
issn	2191-0197
publishDate	2019-12-01
description	Spiro[cyclohexane-1,3’-indoline]-2,2’-diones were easily prepared in good to high yields by the oxidation of N-aryl-N-methyl-2-oxocyclohexane-1-carboxamides in one pot with a short reaction time. The spiroindolinediones could be important for the total synthesis of natural products.
topic	spiro[cyclohexane-1,3’-indoline]-2,2’-diones oxidative cyclization 5-exo cyclization radicals heterocycles
url	https://doi.org/10.1515/hc-2019-0022
work_keys_str_mv	AT katayamashintaro facilesynthesisofspirocyclohexane13indoline22diones AT nishinohiroshi facilesynthesisofspirocyclohexane13indoline22diones
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Facile Synthesis of Spiro[cyclohexane-1,3’-indoline]-2,2’-diones

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