Trifluoromethanesulfonic anhydride–4-(N,N-dimethylamino)pyridine as a reagent combination for effecting Bischler–Napieraiski cyclisation under mild conditions: application to total syntheses of the Amaryllidaceae alkaloids N-methylcrinasiadine, anhydrolycorinone, hippadine and oxoassoanine-Reference-Cited by-同舟云学术

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Trifluoromethanesulfonic anhydride–4-(N,N-dimethylamino)pyridine as a reagent combination for effecting Bischler–Napieraiski cyclisation under mild conditions: application to total syntheses of the Amaryllidaceae alkaloids N-methylcrinasiadine, anhydrolycorinone, hippadine and oxoassoanine

Published:1995 Issue:24 Volume: Page:2551-2553
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Banwell Martin G.,Bissett Brett D.,Busato Stefan,Cowden Cameron J.,Hockless David C. R.,Holman Jeffrey W.,Read Roger W.,Wu Angela W.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1995/C3/C39950002551

Reference32 articles.

1. Correlation of the von Braun, Ritter, Bischler-Napieralski, Beckmann and Schmidt reactions via nitrilium salt intermediates

2. Novel Condensing Agents for Bischler-Napieralski Type Cyclodehydration

3. An improved modification of ritter reaction

4. A new procedure for formylation of less active aromatics

5. A stereoselective total synthesis of (±)-γ-lycorane

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