Novel Products from Bischler-Napieralski Reaction of Arylacetyl-Tryptophan Esters. Synthesis of Spiropentacyclic Indolines Structurally Related to Indole Alkaloids
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919308009792
Reference16 articles.
1. Cyclisation of N-acyltryptamines to spirocyclic indolines
2. Electrophilic substitution in indoles. Part 18. Cyclisation of N-acyltryptamines
3. New evidence for the intermediacy of spiroindolenines in the Bischler–Napieralski cyclization of Nβ-acyltryptamines
4. Intermolecular Trapping by Indole of a Spiroindolenine Intermediated Formed during the Bischler-Napieralski Cyclisation of N-Acetyltryptamine
5. Synthesis of spiropentacyclic indolines by cyclisation of 3,4-dimethoxyphenylacetyltryptamine
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1. Synthesis of Spirocyclic Indolines by Interruption of the Bischler–Napieralski Reaction;Organic Letters;2013-07-05
2. ChemInform Abstract: Novel Products from Bischler-Napieralski Reaction of Arylacetyltryptophan Esters. Synthesis of Spiropentacyclic Indolines Structurally Related to Indole Alkaloids.;ChemInform;2010-08-20
3. Enantioselective Spirocyclizations from Tryptophanol-Derived Oxazolopiperidone Lactams;Organic Letters;2007-06-29
4. Studies on the synthesis of Strychnos indole alkaloids from 2-(3-indolyl)piperidine derivatives. A new synthetic entry to the indolo[3,2-a]quinolizidine system;Arkivoc;2003-07-10
5. Diborane as a reducing agent IX: Reduction of aTris(trifluoroacetyl)enaminospiroindoline;Monatshefte f�r Chemie Chemical Monthly;1997-12
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