Photochemical reactions of naphthyl-vinyl non-conjugated bichromophoric systems

Annoula Kashoulis; Andrew Gilbert; Graham Ellis-Davies

doi:10.1016/S0040-4039(01)81322-8

Photochemical reactions of naphthyl-vinyl non-conjugated bichromophoric systems

Annoula Kashoulis
, Andrew Gilbert
, Graham Ellis-Davies

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

9 Scopus citations

Abstract

2-(1-naphthyl)ethyl vinyl ether undergoes intramolecular 1,2- photocycloaddition whereas the 2-naphthyl isomer yields a product reflecting dimerisation and loss of the elements of acetylene: consistent with such diverse photochemistry, the addition of 2,3-dihydropyran to naphthalene produces only the 1,2-, 1′,2′regioisomer.

Original language	English
Pages (from-to)	2905-2908
Number of pages	4
Journal	Tetrahedron Letters
Volume	25
Issue number	27
DOIs	https://doi.org/10.1016/S0040-4039(01)81322-8
State	Published - 1984
Externally published	Yes

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@article{ef135f46bfda43b3a1459ade4350454d,

title = "Photochemical reactions of naphthyl-vinyl non-conjugated bichromophoric systems",

abstract = "2-(1-naphthyl)ethyl vinyl ether undergoes intramolecular 1,2- photocycloaddition whereas the 2-naphthyl isomer yields a product reflecting dimerisation and loss of the elements of acetylene: consistent with such diverse photochemistry, the addition of 2,3-dihydropyran to naphthalene produces only the 1,2-, 1′,2′regioisomer.",

author = "Annoula Kashoulis and Andrew Gilbert and Graham Ellis-Davies",

year = "1984",

doi = "10.1016/S0040-4039(01)81322-8",

language = "English",

volume = "25",

pages = "2905--2908",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd.",

number = "27",

}

TY - JOUR

T1 - Photochemical reactions of naphthyl-vinyl non-conjugated bichromophoric systems

AU - Kashoulis, Annoula

AU - Gilbert, Andrew

AU - Ellis-Davies, Graham

PY - 1984

Y1 - 1984

N2 - 2-(1-naphthyl)ethyl vinyl ether undergoes intramolecular 1,2- photocycloaddition whereas the 2-naphthyl isomer yields a product reflecting dimerisation and loss of the elements of acetylene: consistent with such diverse photochemistry, the addition of 2,3-dihydropyran to naphthalene produces only the 1,2-, 1′,2′regioisomer.

AB - 2-(1-naphthyl)ethyl vinyl ether undergoes intramolecular 1,2- photocycloaddition whereas the 2-naphthyl isomer yields a product reflecting dimerisation and loss of the elements of acetylene: consistent with such diverse photochemistry, the addition of 2,3-dihydropyran to naphthalene produces only the 1,2-, 1′,2′regioisomer.

UR - https://www.scopus.com/pages/publications/17144426794

U2 - 10.1016/S0040-4039(01)81322-8

DO - 10.1016/S0040-4039(01)81322-8

M3 - Article

AN - SCOPUS:17144426794

SN - 0040-4039

VL - 25

SP - 2905

EP - 2908

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 27

ER -

Photochemical reactions of naphthyl-vinyl non-conjugated bichromophoric systems

Abstract

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