Organocatalytic Redox Isomerization of Electron-Deficient Allylic Alcohols: Synthesis of 1,4-Ketoaldehydes
作者:Keshab Mondal、Buddhadeb Mondal、Subhas Chandra Pan
DOI:10.1021/acs.joc.6b00243
日期:2016.6.3
An organocatalytic redox isomerization strategy has been developed for the synthesis of 1,4-ketoaldehydes. DABCO was found to be the best catalyst for the isomerization of γ-hydroxy enones. With 20 mol % of DABCO as catalyst and DMSO as the solvent high yields have been achieved for different 1,4-ketoaldehydes.
CRAIG, DONALD;DANIELS, KEVIN, TETRAHEDRON LETT., 31,(1990) N4, C. 6441-6444
作者:CRAIG, DONALD、DANIELS, KEVIN
DOI:——
日期:——
PENTABLOCK COPOLYMERS
申请人:3M Innovative Properties Company
公开号:EP3545023B1
公开(公告)日:2020-11-04
BLOCK COPOLYMERS FOR DIRECTED SELF-ASSEMBLY APPLICATIONS
申请人:International Business Machines Corporation
公开号:US20170114246A1
公开(公告)日:2017-04-27
Block copolymers (BCPs) for self-assembly applications comprise a linear fluorinated linking group L′ joining a pair of adjacent blocks. A film layer comprising a BCP, which is disposed on an underlayer and in contact with an atmosphere, is capable of forming a perpendicularly oriented domain pattern when the underlayer is preferentially wetted by one domain of an otherwise identical self-assembled BCP in which all fluorines of L′ are replaced by hydrogen. The BCP can be a low-chi or high-chi BCP. In a preferred embodiment, the BCP comprises a styrene-based first block, and a second block comprises a carbonate and/or ester repeat unit formed by ring opening polymerization of a cyclic carbonate and/or cyclic ester monomer. The linking group L′ has a lower surface energy than each of the polymer blocks.