BISACYL DIGERMANIUM COMPOUNDS, THEIR PREPARATION AND THEIR USE AS PHOTOINITIATOR FOR RADICAL POLYMERIZATION
摘要:
The present invention discloses photoinitiators according to the general formula R
1
R
2
R
3
—Ge—Ge—R
4
R
5
R
6
, wherein each R
1
and R
4
is an acyl group, and the use of such photoinitiators for radical polymerization.
Trichloroisocyanuric Acid, as an Industrial Chemical, Promotes Transthioacetalization of Diacetals of 2,2-Bis (Hydroxymethyl)-1,3-propanediol and Cleavage of Thioacetals
Trichloroisocyanuric acid has been used as a mild, efficient, and new catalyst for transthioacetalization of diacetals of 2,2-bis (hydroxymethyl)-1,3-propanediol in CH 2 Cl 2 at room temperature. A clean, easy, and general method for efficientdeprotection of thioacetals to their corresponding carbonyl compounds using trichloroisocyanuric acid/silica gel and water system also is described.
2,4,4,6-Tetrabromo-2,5-cyclohexadienone (TABCO), N-Bromosuccinimide (NBS) and Bromine as Efficient Catalysts for Dithioacetalization and Oxathioacetalization of Carbonyl Compounds and Transdithioacetalization Reactions
作者:Nasser Iranpoor、Habib Firouzabadi、Hamid Reza Shaterian、M. A. Zolfigol
DOI:10.1080/10426500211712
日期:2002.5.1
6-tetrabromo-2,5-cyclohexadienone (TABCO), N-bromosuccinimide (NBS), and bromine as efficient catalysts for conversion of carbonyl compounds to their cyclic and acyclic dithioacetals and 1,3-oxathiolanes under mild reaction conditions are described. These catalysts are also used for efficient transdithioacetalization of acetals, diacetals, ketals, acylals, enamines, hydrazones, and oximes with high
Aluminum hydrogen sulfate [Al(HSO4)3] as an efficient catalyst for the preparation of thioacetals
作者:Majid Ghashang
DOI:10.1007/s11164-012-0802-8
日期:2013.7
Aluminum hydrogen sulfate, as a heterogeneous solid acid catalyst, has been used for the mild conversion of carbonyl compounds to their thioacetals using 1,2- and 1,3-dithiol under ambient conditions with short reaction times in high to excellent yield in acetonitrile as solvent.
Oxidative [1,2]-Brook Rearrangements Exploiting Single-Electron Transfer: Photoredox-Catalyzed Alkylations and Arylations
作者:Yifan Deng、Qi Liu、Amos B. Smith
DOI:10.1021/jacs.7b05165
日期:2017.7.19
Oxidative [1,2]-Brook rearrangements via hypervalent silicon intermediates induced by photoredox-catalyzed single-electron transfer have been achieved, permitting the formation of reactive radical species that can engage in alkylations and arylations.
An Organocatalytic Process for the Hydrolytic Cleavage of Dithianes Mediated by Imidazolium Ions: No Harsh Agents Required
作者:Lauren Myles、Nicholas Gathergood、Stephen J. Connon
DOI:10.1002/ejoc.201402947
日期:2015.1
A new, organocatalytic approach to the hydrolytic deprotection of dithianes has been developed involving a low-toxicity imidazolium-ion-based catalyst in an aqueous medium. A complimentary solvent-free method without added water and involving a sacrificial aldehyde is also reported. The catalyst does not appear to operate by a specific-acid catalysis mechanism.