Highly Selective β-Hydride Elimination in Pd-Catalyzed Decarboxylative Heck-Type Reaction
摘要:
A variety of beta-aryl ketones and aldehydes were facilely synthesized via a Pd(II)/Ag2CO3-mediated decarboxylative Heck type reaction between readily available benzoic acid derivatives and allylic alcohols under mild conditions. The control experiments indicated that this transformation may proceed via a hydrogen migration process.
Pyrimidinone Derivatives and Their Use in the Treatment of Atherosclerosis
申请人:Elliott Leonard Richard
公开号:US20060241126A1
公开(公告)日:2006-10-26
Compounds of formula (I):
are inhibitors of the enzyme Lp-PLA
2
and are of use in therapy, in particular for treating atherosclerosis.
公式为(I)的化合物是Lp-PLA2酶的抑制剂,可用于治疗,特别是用于治疗动脉粥样硬化。
Bi-functional complexes and methods for making and using such complexes
申请人:Gouliaev Alex Haahr
公开号:US11225655B2
公开(公告)日:2022-01-18
The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.
BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES
申请人:Nuevolution A/S
公开号:EP2558577A1
公开(公告)日:2013-02-20
BI-FUNCTINAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES
申请人:Gouliaev Alex Haahr
公开号:US20130281324A1
公开(公告)日:2013-10-24
The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.