Passerini/Tsuji-Trost strategies towards achieving lactams and cyclopentane derivatives

Marie Cordier; Aurélie Dos Santos; Laurent El Kaïm; Noisette Narboni

doi:10.1039/c5cc00584a

Passerini/Tsuji-Trost strategies towards achieving lactams and cyclopentane derivatives

Marie Cordier
, Aurélie Dos Santos
, Laurent El Kaïm
, Noisette Narboni

CNRS
Unité Chimie et Procédés

Résultats de recherche: Contribution à un journal › Article › Revue par des pairs

13 Citations (Scopus)

Résumé

The Passerini reaction of α,β-unsaturated aldehydes affords suitable substrates for the Tsuji-Trost reaction with various carbon based-nucleophiles. The resulting α,β-unsaturated amides may be cyclized to lactams or converted into cyclopentane derivatives if bis-nucleophiles are used in the Tsuji-Trost step.

langue originale	Anglais
Pages (de - à)	6411-6414
Nombre de pages	4
journal	Chemical Communications
Volume	51
Numéro de publication	29
Les DOIs	https://doi.org/10.1039/c5cc00584a
état	Publié - 14 avr. 2015
Modification externe	Oui

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10.1039/c5cc00584a

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title = "Passerini/Tsuji-Trost strategies towards achieving lactams and cyclopentane derivatives",

abstract = "The Passerini reaction of α,β-unsaturated aldehydes affords suitable substrates for the Tsuji-Trost reaction with various carbon based-nucleophiles. The resulting α,β-unsaturated amides may be cyclized to lactams or converted into cyclopentane derivatives if bis-nucleophiles are used in the Tsuji-Trost step.",

author = "Marie Cordier and \{Dos Santos\}, Aur{\'e}lie and \{El Ka{\"i}m\}, Laurent and Noisette Narboni",

note = "Publisher Copyright: {\textcopyright} The Royal Society of Chemistry 2015.",

year = "2015",

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doi = "10.1039/c5cc00584a",

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T1 - Passerini/Tsuji-Trost strategies towards achieving lactams and cyclopentane derivatives

AU - Cordier, Marie

AU - Dos Santos, Aurélie

AU - El Kaïm, Laurent

AU - Narboni, Noisette

PY - 2015/4/14

Y1 - 2015/4/14

N2 - The Passerini reaction of α,β-unsaturated aldehydes affords suitable substrates for the Tsuji-Trost reaction with various carbon based-nucleophiles. The resulting α,β-unsaturated amides may be cyclized to lactams or converted into cyclopentane derivatives if bis-nucleophiles are used in the Tsuji-Trost step.

AB - The Passerini reaction of α,β-unsaturated aldehydes affords suitable substrates for the Tsuji-Trost reaction with various carbon based-nucleophiles. The resulting α,β-unsaturated amides may be cyclized to lactams or converted into cyclopentane derivatives if bis-nucleophiles are used in the Tsuji-Trost step.

U2 - 10.1039/c5cc00584a

DO - 10.1039/c5cc00584a

M3 - Article

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EP - 6414

JO - Chemical Communications

JF - Chemical Communications

IS - 29

ER -

Passerini/Tsuji-Trost strategies towards achieving lactams and cyclopentane derivatives

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