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

Research output: Contribution to journal › Article › peer-review

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.

Original language	English
Pages (from-to)	6411-6414
Number of pages	4
Journal	Chemical Communications
Volume	51
Issue number	29
DOIs	https://doi.org/10.1039/c5cc00584a
Publication status	Published - 14 Apr 2015
Externally published	Yes

Access to Document

10.1039/c5cc00584a

Cite this

@article{ad1e01eb08264891b60c5936e7bd5366,

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",

month = apr,

day = "14",

doi = "10.1039/c5cc00584a",

language = "English",

volume = "51",

pages = "6411--6414",

journal = "Chemical Communications",

issn = "1359-7345",

number = "29",

}

TY - JOUR

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

N1 - Publisher Copyright: © The Royal Society of Chemistry 2015.

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

AN - SCOPUS:84961291580

SN - 1359-7345

VL - 51

SP - 6411

EP - 6414

JO - Chemical Communications

JF - Chemical Communications

IS - 29

ER -

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

Abstract

Access to Document

Fingerprint

Cite this