OXIDATION OF ACETONE UNDER BAEYER-VILLIGER CONDITIONS - EVIDENCE FOR FORMATION OF ACETONE CARBONYL OXIDE OR ITS ISOMERIC DIOXIRANE

被引:31
作者
MURRAY, RW
RAMACHANDRAN, V
机构
[1] Department of Chemistry, University of Missouri — St. Louis, St Louis, Missouri
关键词
D O I
10.1111/j.1751-1097.1979.tb07134.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Abstract— Oxidation of acetone under Baeyer‐Villager conditions produces a new species which is capable of epoxidizing olefins. It is suggested that this intermediate is acetone carbonyl oxide or its isomer dimethyldioxirane. Copyright © 1979, Wiley Blackwell. All rights reserved
引用
收藏
页码:187 / 189
页数:3
相关论文
共 11 条
[1]  
EDWARDS JO, PHOTOCHEM PHOTOBIOL
[2]   MECHANISMS OF GAS-PHASE AND LIQUID-PHASE OZONOLYSIS [J].
HARDING, LB ;
GODDARD, WA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1978, 100 (23) :7180-7188
[3]  
Hassall C.H., 1957, ORG REACT, V9, P73
[4]   OXIDATION OF DIAZO-COMPOUNDS WITH SINGLET OXYGEN - FORMATION OF OZONIDES [J].
HIGLEY, DP ;
MURRAY, RW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1974, 96 (10) :3330-3332
[5]   EPOXIDATION OF OLEFINS WITH CARBONYL OXIDES [J].
HINRICHS, TA ;
RAMACHANDRAN, V ;
MURRAY, RW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1979, 101 (05) :1282-1284
[6]   IDENTIFICATION OF DIOXIRANE (H2COO) IN OZONE-OLEFIN REACTIONS VIA MICROWAVE SPECTROSCOPY [J].
LOVAS, FJ ;
SUENRAM, RD .
CHEMICAL PHYSICS LETTERS, 1977, 51 (03) :453-456
[7]   OZONIDES FROM PHOTOOXIDATION OF DIPHENYLDIAZOMETHANE IN PRESENCE OF ALDEHYDES [J].
MURRAY, RW ;
SUZUI, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1971, 93 (19) :4963-&
[8]   MECHANISM OF OZONOLYSIS - NEW ROUTE TO OZONIDES [J].
MURRAY, RW ;
SUZUI, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1973, 95 (10) :3343-3348
[9]  
MURRAY RW, 1972, OZONE REACTIONS ORGA, P9
[10]  
SMITH PAS, 1963, MOL REARRANGEMENTS, P568