Macrocyclic ethers by free radical cyclizations

Annie Philippon; Jingchao Tao; David Tétard; Marie Degueil-Castaing; Bernard Maillard

doi:10.1080/00397919708004135

Macrocyclic ethers by free radical cyclizations

Annie Philippon, Jingchao Tao, David Tétard, Marie Degueil-Castaing, Bernard Maillard^*

^*Corresponding author for this work

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

10 Citations (Scopus)

Abstract

Tin hydride reduction of ω-iodo-polyoxaalkyl acrylates 1 using syringe pump addition of both reactants to a solution of AIBN in benzene at 80°C afforded the corresponding cyclic polyethers in excellent yields.

Original language	English
Pages (from-to)	2651-2682
Number of pages	32
Journal	Synthetic Communications
Volume	27
Issue number	15
DOIs	https://doi.org/10.1080/00397919708004135
Publication status	Published - 1997
Externally published	Yes

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10.1080/00397919708004135

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title = "Macrocyclic ethers by free radical cyclizations",

abstract = "Tin hydride reduction of ω-iodo-polyoxaalkyl acrylates 1 using syringe pump addition of both reactants to a solution of AIBN in benzene at 80°C afforded the corresponding cyclic polyethers in excellent yields.",

author = "Annie Philippon and Jingchao Tao and David T{\'e}tard and Marie Degueil-Castaing and Bernard Maillard",

year = "1997",

doi = "10.1080/00397919708004135",

language = "English",

volume = "27",

pages = "2651--2682",

journal = "Synthetic Communications",

issn = "0039-7911",

publisher = "Taylor \& Francis",

number = "15",

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TY - JOUR

T1 - Macrocyclic ethers by free radical cyclizations

AU - Philippon, Annie

AU - Tao, Jingchao

AU - Tétard, David

AU - Degueil-Castaing, Marie

AU - Maillard, Bernard

PY - 1997

Y1 - 1997

N2 - Tin hydride reduction of ω-iodo-polyoxaalkyl acrylates 1 using syringe pump addition of both reactants to a solution of AIBN in benzene at 80°C afforded the corresponding cyclic polyethers in excellent yields.

AB - Tin hydride reduction of ω-iodo-polyoxaalkyl acrylates 1 using syringe pump addition of both reactants to a solution of AIBN in benzene at 80°C afforded the corresponding cyclic polyethers in excellent yields.

UR - https://www.scopus.com/pages/publications/0000406891

U2 - 10.1080/00397919708004135

DO - 10.1080/00397919708004135

M3 - Article

AN - SCOPUS:0000406891

SN - 0039-7911

VL - 27

SP - 2651

EP - 2682

JO - Synthetic Communications

JF - Synthetic Communications

IS - 15

ER -

Macrocyclic ethers by free radical cyclizations

Abstract

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