Substituent Effect in Photochemistry of Carbonyl Compounds: α-Halovalerophenones

Sungsu Cho; Bong Ser Park

doi:10.5012/bkcs.2004.25.1.042

Substituent Effect in Photochemistry of Carbonyl Compounds: α-Halovalerophenones

Sungsu Cho, Bong Ser Park

Department of Chemistry

Dongguk University

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

12 Scopus citations

Abstract

Valerophenones containing a substituent at alpha position to the carbonyl group show the remarkable substituent effects on their photochemical reactions. α-Bromovalerophenone gives only the C-Br bond cleavage products, but the α-chlorovalerophenone follows the classical Norrish/Yang reaction pathway predominantly.

Original language	English
Pages (from-to)	42-44
Number of pages	3
Journal	Bulletin of the Korean Chemical Society
Volume	25
Issue number	1
DOIs	https://doi.org/10.5012/bkcs.2004.25.1.042
State	Published - 20 Jan 2004

Keywords

Halo ketone
Photochemistry
Substituent effect

Access to Document

10.5012/bkcs.2004.25.1.042

Cite this

@article{fae2727b559a4af697b623392af249b5,

title = "Substituent Effect in Photochemistry of Carbonyl Compounds: α-Halovalerophenones",

abstract = "Valerophenones containing a substituent at alpha position to the carbonyl group show the remarkable substituent effects on their photochemical reactions. α-Bromovalerophenone gives only the C-Br bond cleavage products, but the α-chlorovalerophenone follows the classical Norrish/Yang reaction pathway predominantly.",

keywords = "Halo ketone, Photochemistry, Substituent effect",

author = "Sungsu Cho and Park, {Bong Ser}",

year = "2004",

month = jan,

day = "20",

doi = "10.5012/bkcs.2004.25.1.042",

language = "English",

volume = "25",

pages = "42--44",

journal = "Bulletin of the Korean Chemical Society",

issn = "0253-2964",

publisher = "Wiley-Blackwell",

number = "1",

}

TY - JOUR

T1 - Substituent Effect in Photochemistry of Carbonyl Compounds

T2 - α-Halovalerophenones

AU - Cho, Sungsu

AU - Park, Bong Ser

PY - 2004/1/20

Y1 - 2004/1/20

N2 - Valerophenones containing a substituent at alpha position to the carbonyl group show the remarkable substituent effects on their photochemical reactions. α-Bromovalerophenone gives only the C-Br bond cleavage products, but the α-chlorovalerophenone follows the classical Norrish/Yang reaction pathway predominantly.

AB - Valerophenones containing a substituent at alpha position to the carbonyl group show the remarkable substituent effects on their photochemical reactions. α-Bromovalerophenone gives only the C-Br bond cleavage products, but the α-chlorovalerophenone follows the classical Norrish/Yang reaction pathway predominantly.

KW - Halo ketone

KW - Photochemistry

KW - Substituent effect

UR - http://www.scopus.com/inward/record.url?scp=1642544083&partnerID=8YFLogxK

U2 - 10.5012/bkcs.2004.25.1.042

DO - 10.5012/bkcs.2004.25.1.042

M3 - Article

AN - SCOPUS:1642544083

SN - 0253-2964

VL - 25

SP - 42

EP - 44

JO - Bulletin of the Korean Chemical Society

JF - Bulletin of the Korean Chemical Society

IS - 1

ER -

Substituent Effect in Photochemistry of Carbonyl Compounds: α-Halovalerophenones

Abstract

Keywords

Access to Document

Other files and links

Fingerprint

Cite this