Cyclisation reactions of N-cinnamoyl-9-aminoanthracenes
Author:
Affiliation:
1. Department of Chemistry
2. University College London
3. London, UK
Abstract
N-Cinnamoyl-9-aminoanthracenes cyclise with PPA or triflic acid to form novel 2-azahexacyclo[10.6.6.01,5.06,11.013,18.019,24]tetracosa-6(11),7,9,13,15,17,19(24),20,22-nonaen-3-ones.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB00411F
Reference17 articles.
1. The triflic acid-mediated cyclisation of N-benzylcinnamanilides
2. The Triflic Acid-Mediated Cyclization Reactions of N-Cinnamoyl-1-Naphthylamines
3. Asymmetric control in Diels–Alder cycloadditions of chiral 9-aminoanthracenes by relay of stereochemical information
4. Ueber die Einwirkung von Salpetersäure auf Anthracen
5. Conformation of Secondary Amides. A Predictive Algorithm That Correlates DFT-Calculated Structures and Experimental Proton Chemical Shifts
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1. Proton‐ and halogen‐induced cyclizations of 2‐(3‐butenyl)quinazolin‐4( 3 H)‐ones in the synthesis of pyrrolo[2,1‐ b ]‐ and pyrrolo[1,2‐ а ]quinazolinone derivatives;Journal of Heterocyclic Chemistry;2022-11-20
2. Trifluoromethanesulfonic acid in organic synthesis;Russian Journal of Organic Chemistry;2017-04
3. ChemInform Abstract: Cyclization Reactions of N-Cinnamoyl-9-aminoanthracenes.;ChemInform;2014-10-10
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