Multiple radical additions: An expedient entry into complex frameworks

Derek H.R. Barton; Elisabeth Da Silva; Samir Z. Zard

doi:10.1039/C39880000285

Multiple radical additions: An expedient entry into complex frameworks

Derek H.R. Barton
, Elisabeth Da Silva
, Samir Z. Zard

Texas A&M University
Laboratoire de Synthèse Organique

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

Résumé

Irradiation of N-hydroxy-2-thiopyridone esters of suitable γ,δ-unsaturated carboxylic acids in the presence of an electron deficient alkene produces complex bicyclic systems by a multiple radical addition chain mechanism.

langue originale	Anglais
Pages (de - à)	285-287
Nombre de pages	3
journal	Journal of the Chemical Society, Chemical Communications
Numéro de publication	4
Les DOIs	https://doi.org/10.1039/C39880000285
état	Publié - 1 janv. 1988
Modification externe	Oui

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10.1039/C39880000285

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@article{7f8464316150462da991cdc7e8a38ca3,

title = "Multiple radical additions: An expedient entry into complex frameworks",

abstract = "Irradiation of N-hydroxy-2-thiopyridone esters of suitable γ,δ-unsaturated carboxylic acids in the presence of an electron deficient alkene produces complex bicyclic systems by a multiple radical addition chain mechanism.",

author = "Barton, \{Derek H.R.\} and \{Da Silva\}, Elisabeth and Zard, \{Samir Z.\}",

year = "1988",

month = jan,

day = "1",

doi = "10.1039/C39880000285",

language = "English",

pages = "285--287",

journal = "Journal of the Chemical Society, Chemical Communications",

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T1 - Multiple radical additions

T2 - An expedient entry into complex frameworks

AU - Barton, Derek H.R.

AU - Da Silva, Elisabeth

AU - Zard, Samir Z.

PY - 1988/1/1

Y1 - 1988/1/1

N2 - Irradiation of N-hydroxy-2-thiopyridone esters of suitable γ,δ-unsaturated carboxylic acids in the presence of an electron deficient alkene produces complex bicyclic systems by a multiple radical addition chain mechanism.

AB - Irradiation of N-hydroxy-2-thiopyridone esters of suitable γ,δ-unsaturated carboxylic acids in the presence of an electron deficient alkene produces complex bicyclic systems by a multiple radical addition chain mechanism.

UR - https://www.scopus.com/pages/publications/37049083104

U2 - 10.1039/C39880000285

DO - 10.1039/C39880000285

M3 - Article

AN - SCOPUS:37049083104

SN - 0022-4936

SP - 285

EP - 287

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 4

ER -

Multiple radical additions: An expedient entry into complex frameworks

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