Synthesis of spiro[cycloalkane-1,3'-[3H]indoles] from cycloalkane-carbaldehydes. Acid-catalyzed rearrangement to cycloalkano[b]indoles

DOI: 10.1002/jhet.5570220512

Source and publish data:

Journal of Heterocyclic Chemistry p. 1207 - 1210 (1985)

Update date:2022-08-03

Topics:

Authors:

Rodriguez

Benito Benito

Temprano

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1002/jhet.5570220512

Full text of DOI:10.1002/jhet.5570220512

Products guided by the article

Product name:Spiro[cycloheptane-1,3'-[3H]indole]

Cas No:16914-67-3

R&D Labs maybe for 16914-67-3

Taizhou Crene Biotechnology co.ltd

Contact:86-576-88813233 88205808

Address:Economic Developed Zone of Taizhou Zhejiang China
Hangzhou Maytime Bio-Tech Co.,Ltd.

website:http://www.maytime.com.cn

Contact:+86-571-88925295 88920965

Address:NO.2-1701 Ganghui Central Ningwei Street, Xiaoshan Hangzhou Zhejiang China
Lianyungang Ningkang Chemical Co., Ltd

Contact:.+86-518-88588008

Address:http://www.chemnk.com
Shanghai Hanhong Scientific Co.,Ltd.

website:http://www.chemvia.com

Contact:+86-21-64541543,54280654,13918533501

Address:Jiachuan Road 245
MINS GROUP CO.,LIMITED

Contact:18669908765

Address:Zibo City, Shandong Province, P.R.China

Relevant to this article

ALKALOIDS OF Nitraria komarovii. XI. STRUCTURE OF KOMAVICINE AND THE PRODUCTS OF THE DEHYDROGENATION OF THE NITRARINE METHOD OF DEHYDROGENATION IN THE QUINOLINYL-β-CARBOLINE SERIES

Doi:10.1007/BF00631008
(1993)
Doi:10.1021/ja01098a514
(1953)
(Phenylsulfonyl)allenes as substrates for cycloaddition reactions: Intramolecular cyclizations onto unactivated alkenes

Doi:10.1021/ja00132a005
(1995)
Cyclopentannulations Leading to the Synthesis of Bicyclic Conjugated Enediones

Doi:10.1021/jo00121a035
(1995)
The reactivity of N,N-dialkyl-N-(3-phenylsulfinyltetrahydrofuran-2-ylidene) ammonium bromide

Doi:10.1007/s11172-007-0240-8
(2007)
Doi:10.1021/jo00800a035
(1971)

Article Doi