Photoinduced one pot transformation of 2-phenyl-4-ethylidene-5(4H)- oxazolone and allylic alcohols to γ, δ-unsaturated N-henzoyl amides

Bong Ser Park; Chul Min Oh; Keun Ho Chun; Jong Ook Lee

doi:10.1016/S0040-4039(98)02232-1

Photoinduced one pot transformation of 2-phenyl-4-ethylidene-5(4H)- oxazolone and allylic alcohols to γ, δ-unsaturated N-henzoyl amides

Bong Ser Park
, Chul Min Oh
, Keun Ho Chun
, Jong Ook Lee

Department of Chemistry

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

15 Scopus citations

Abstract

Photolysis of 2-Phenyl-4-ethylidene-5(4H)-oxazolones in the presence of allylic alcohols resulted in a navel one-pot transformation to γ,δ- unsaturated N-benzoyl amides via decarbonylation, nucleophilic addition of allylic alcohols, photoinduced hydrogen transfer and the Claisen rearrangement.

Original language	English
Pages (from-to)	9711-9714
Number of pages	4
Journal	Tetrahedron Letters
Volume	39
Issue number	52
DOIs	https://doi.org/10.1016/S0040-4039(98)02232-1
State	Published - 24 Dec 1998

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title = "Photoinduced one pot transformation of 2-phenyl-4-ethylidene-5(4H)- oxazolone and allylic alcohols to γ, δ-unsaturated N-henzoyl amides",

abstract = "Photolysis of 2-Phenyl-4-ethylidene-5(4H)-oxazolones in the presence of allylic alcohols resulted in a navel one-pot transformation to γ,δ- unsaturated N-benzoyl amides via decarbonylation, nucleophilic addition of allylic alcohols, photoinduced hydrogen transfer and the Claisen rearrangement.",

author = "Park, \{Bong Ser\} and Oh, \{Chul Min\} and Chun, \{Keun Ho\} and Lee, \{Jong Ook\}",

year = "1998",

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doi = "10.1016/S0040-4039(98)02232-1",

language = "English",

volume = "39",

pages = "9711--9714",

journal = "Tetrahedron Letters",

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T1 - Photoinduced one pot transformation of 2-phenyl-4-ethylidene-5(4H)- oxazolone and allylic alcohols to γ, δ-unsaturated N-henzoyl amides

AU - Park, Bong Ser

AU - Oh, Chul Min

AU - Chun, Keun Ho

AU - Lee, Jong Ook

PY - 1998/12/24

Y1 - 1998/12/24

N2 - Photolysis of 2-Phenyl-4-ethylidene-5(4H)-oxazolones in the presence of allylic alcohols resulted in a navel one-pot transformation to γ,δ- unsaturated N-benzoyl amides via decarbonylation, nucleophilic addition of allylic alcohols, photoinduced hydrogen transfer and the Claisen rearrangement.

AB - Photolysis of 2-Phenyl-4-ethylidene-5(4H)-oxazolones in the presence of allylic alcohols resulted in a navel one-pot transformation to γ,δ- unsaturated N-benzoyl amides via decarbonylation, nucleophilic addition of allylic alcohols, photoinduced hydrogen transfer and the Claisen rearrangement.

UR - https://www.scopus.com/pages/publications/0032564536

U2 - 10.1016/S0040-4039(98)02232-1

DO - 10.1016/S0040-4039(98)02232-1

M3 - Article

AN - SCOPUS:0032564536

SN - 0040-4039

VL - 39

SP - 9711

EP - 9714

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 52

ER -

Photoinduced one pot transformation of 2-phenyl-4-ethylidene-5(4H)- oxazolone and allylic alcohols to γ, δ-unsaturated N-henzoyl amides

Abstract

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