A simple synthesis of spiro-C6-annulated hydrocyclopenta[g]indole derivatives

A series of new spiro-C6-annulated hydrogenated cyclopenta[g]indoles (5) was prepared by applying Madelung method to the appropriate 4-(N-acetylamino)-1-spiroindanes (9), synthesised via acid-catalysed intramolecular rearrangement of 1-acetyl-3,4-dihydrospiro[quinoline-2,1′-cycloalkanes] (8). © 2002 Elsevier Science Ltd. All rights reserved.

Authors
Kouznetsov V.1 , Zubkov F. 2 , Palma A.1 , Restrepo G.1
Publisher
Elsevier Ltd
Number of issue
26
Language
English
Pages
4707-4709
Status
Published
Number
21609
Volume
43
Year
2002
Organizations
  • 1 Laboratory of Fine Organic Synthesis, Research Center for Biomolecules, Industrial University of Santander, A.A. 678, Bucaramanga, Colombia
  • 2 Department of Organic Chemistry, Russian Peoples Friendship University, Moscow 117923, Russian Federation
Keywords
Aminoindanes; Hydrocyclopenta[g]indoles; Madelung synthesis; Trikentrins
Date of creation
19.10.2018
Date of change
16.08.2021
Short link
https://repository.rudn.ru/en/records/article/record/244/
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