A Significant Effect of Triflic Acid on the Hypervalent λn-Iodane-Mediated Fragmentation of the Tertiary Cyclopropanol System
摘要:
Trifluoromethanesulfonic acid enhanced the ring cleavage in the reaction of silyl tertiary cyclopropyl ethers with phenyliodine(III) diacetate in a catalytic amount.
A Significant Effect of Triflic Acid on the Hypervalent λn-Iodane-Mediated Fragmentation of the Tertiary Cyclopropanol System
摘要:
Trifluoromethanesulfonic acid enhanced the ring cleavage in the reaction of silyl tertiary cyclopropyl ethers with phenyliodine(III) diacetate in a catalytic amount.
Efficient Fragmentation of the Tertiary Cyclopropanol System: Oxidation of 1-(Trimethylsiloxy)bicyclo[n.1.0]alkanes and Analogues By Using Phenyliodine(III) Diacetate
作者:M Kirihara
DOI:10.1016/00404-0399(50)1427j-
日期:1995.9.18
Hypervalent λn-iodane-mediated fragmentation of tertiary cyclopropanol systems
The oxidation of tertiary cyclopropyl silyl ethers with hypervalent lambda(n)-iodanes caused fragmentation which produced alkenoic acids or esters. (C) 1998 Elsevier Science Ltd. All rights reserved.
A Significant Effect of Triflic Acid on the Hypervalent λ<sup>n</sup>-Iodane-Mediated Fragmentation of the Tertiary Cyclopropanol System
Trifluoromethanesulfonic acid enhanced the ring cleavage in the reaction of silyl tertiary cyclopropyl ethers with phenyliodine(III) diacetate in a catalytic amount.