A new rearrangement of N-trifluoroacetoxyammonium salt under Polonovski–Potier reaction conditions: aziridinium versus iminium formation-Reference-Cited by-同舟云学术

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A new rearrangement of N-trifluoroacetoxyammonium salt under Polonovski–Potier reaction conditions: aziridinium versus iminium formation

Published:2001-05 Issue:19 Volume:42 Page:3291-3293
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Thomas O.P,Zaparucha A,Husson H.-P

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference10 articles.

1. Partial synthesis of camptothecin analogs. Part 1: Pyrroloquinolone and pyrroloquinoline derivatives

2. Organic Reactions;Grierson,1990

3. A New Potential Acyl Iminium Ion for the Asymmetric Synthesis of Piperidine Derivatives

4. Synthesis and chemistry of 5,6-dihydropyridinium salt adducts. Synthons for general electrophilic and nucleophilic substitution of the piperidine ring system

5. Acid-catalysed Red-Ox Rearrangement of a Hemiketal

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1. Polonovski–Potier Reaction;Name Reactions;2021

2. 6.17 Polonovski- and Pummerer-type Reactions and the Nef Reaction;Comprehensive Organic Synthesis II;2014

3. Polonovski–Potier reaction;Name Reactions;2014

4. Polonovski Reaction;Comprehensive Organic Name Reactions and Reagents;2010-09-15

5. Polonovski–Potier reaction;Name Reactions;2009

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