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Journal ArticleDOI

2-Substituted Glutarimides via Preformed Wittig Reagents

M. J. Wanner, +1 more
- 01 Jan 1988 - 
- Vol. 1988, Iss: 04, pp 325-327
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TLDR
Synthese des composes du titre par reaction de Wittig entre le dioxo-2,6 P,P,P-triphenyl phosphonio-3 piperidinure-3 et des aldehydes ou des aldoses as mentioned in this paper.
Abstract
Synthese des composes du titre par reaction de Wittig entre le dioxo-2,6 P,P,P-triphenyl phosphonio-3 piperidinure-3 et des aldehydes ou des aldoses

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Journal ArticleDOI

An isocyanide-based three-component reaction: synthesis of fully substituted N-alkyl-2-triphenylphosphoranylidene glutarimides

TL;DR: In this article, a three-component condensation reaction between an isocyanide, an electron-deficient acetylenic ester and (ethoxycarbonylmethyl)triphenylphosphonium bromide efficiently provides fully substituted N-alkyl-2.
Book ChapterDOI

Synthesis of Phosphonium Ylides

TL;DR: In this paper, carbenes and carbenoids are added to tertiary phosphines to obtain alkylidenephosphoranes which carry one or two halogen atoms at the α-carbon atom.
Journal ArticleDOI

Biomimetic synthesis of nitraria alkaloids: stereoselective spirocyclization reactions

TL;DR: The Michael-induced spirocyclization of 2-alkylidene glutarimides offers a highly stereoselective method for a biomimetic synthesis of nitamine and for the construction of the nitraramine carbon-nitrogen framework as discussed by the authors.
Journal ArticleDOI

A simple protocol for the synthesis of a piperidine-2,6-dione framework from Baylis―Hillman adducts

TL;DR: In this paper, the Baylis-Hillman reaction was used to transform 3-hydroxy-2-methylenealkanenitriles into 4-aryl-3-methylidenepiperidine-2,6-diones in a simple one-pot multi-step process involving Johnson-Claisen rearrangement, partial hydrolysis, and cyclization.
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