Synthesis of (±)-Lasubine II Using N
-Methoxyamines
摘要:
AbstractThe synthesis of (±)‐lasubine II has been achieved through a three‐component allylation capitalizing on the unique properties of N‐methoxyamines. This reaction enabled the installation of all the carbon atoms of lasubine II in a single operation. The N‐methoxy group was efficiently used for the subsequent nitrone formation. A single‐step cyclization of isoxazolidines or N‐methoxyamines to form functionalized piperidine rings was also developed.
Simple Primary Anilines as Iminium Catalysts for the Epoxidation of α-Substituted Acroleins
作者:Anniina Erkkilä、Petri M. Pihko、Melanie-Rose Clarke
DOI:10.1002/adsc.200700048
日期:2007.4.2
Simple ortho-alkylated anilines have been shown to be excellent iminiumcatalysts for the epoxidation reaction of α-substitutedacroleins. A range of different α-substitutedacroleins give the epoxide products in good to excellent yields and good chemoselectivity.
Compositions and Methods for Treating Neoplasia, Inflammatory Disease and Other Disorders
申请人:Dana-Farber Cancer Institute, Inc.
公开号:US20150150885A1
公开(公告)日:2015-06-04
The invention features compositions and methods for treating or preventing a neoplasia. More specifically, the invention provides compositions and methods for disrupting the interaction of a BET family polypeptide comprising a bromodomain with chromatin (e.g., disrupting a bromodomain interaction with an acetyl-lysine modification present on a histone N-terminal tail).
US9320741B2
申请人:——
公开号:US9320741B2
公开(公告)日:2016-04-26
Synthesis of (±)-Lasubine II Using <i>N</i>
-Methoxyamines
AbstractThe synthesis of (±)‐lasubine II has been achieved through a three‐component allylation capitalizing on the unique properties of N‐methoxyamines. This reaction enabled the installation of all the carbon atoms of lasubine II in a single operation. The N‐methoxy group was efficiently used for the subsequent nitrone formation. A single‐step cyclization of isoxazolidines or N‐methoxyamines to form functionalized piperidine rings was also developed.
Microwave-assisted selective protection of glutaraldehyde and its symmetrical derivatives as monoacetals and -thioacetals
Six monoprotected acetals and -thioacetals of glutaradehyde and itssymmetrical dimethyl derivatives were synthesized. Microwave-assisted heating proved to be a substantially more selective method for monoprotection than conventional heating. All reactions were efficient and only traces of diprotected material were formed.