Direct Catalytic Anti-Markovnikov Hydroetherification of Alkenols
摘要:
A direct intramolecular anti-Markovnikov hydroetherification reaction of alkenols is described. By employing Catalytic quantities of commercially available 9-mesityl-10-methylacridinium perchlorate and 2-phenyl-malononitrile as a redox-cycling source of a H-atom, we report the anti-Markovnikov hydroetherification of alkenes with complete regioselectivity, In addition, we present results demonstrating that this novel catalytic system can be applied to the anti-Markovnikov hydrolactonization of alkenoic acids.
2-Isopropyl-5-methyloxepan und dessen Verwendung als Riechstoff
申请人:Symrise GmbH & Co. KG
公开号:EP1923389A1
公开(公告)日:2008-05-21
Beschrieben wird 2-Isopropyl-5-methyloxepan der Formel A
und dessen Verwendung als Riechstoff.
所述的是式 A 的 2-异丙基-5-甲基氧杂环庚烷
及其作为香水剂的用途。
DIRECT ANTI-MARKOVNIKOV ADDITION OF ACIDS TO ALKENES
申请人:The University of North Carolina at Chapel Hill
公开号:US20150133680A1
公开(公告)日:2015-05-14
A method of making an anti-Markovnikov addition product is carried out by reacting an acid with an alkene or alkyne in a dual catalyst reaction system to the exclusion of oxygen to produce said anti-Markovnikov addition product; the dual catalyst reaction system comprising a single electron oxidation catalyst in combination with a hydrogen atom donor catalyst. Compositions useful for carrying out such methods are also described.
US9365530B2
申请人:——
公开号:US9365530B2
公开(公告)日:2016-06-14
Direct Catalytic Anti-Markovnikov Hydroetherification of Alkenols
作者:David S. Hamilton、David A. Nicewicz
DOI:10.1021/ja309635w
日期:2012.11.14
A direct intramolecular anti-Markovnikov hydroetherification reaction of alkenols is described. By employing Catalytic quantities of commercially available 9-mesityl-10-methylacridinium perchlorate and 2-phenyl-malononitrile as a redox-cycling source of a H-atom, we report the anti-Markovnikov hydroetherification of alkenes with complete regioselectivity, In addition, we present results demonstrating that this novel catalytic system can be applied to the anti-Markovnikov hydrolactonization of alkenoic acids.