Coupling reactions of acyl chlorides with terminal alkynes and triarylbismuths catalyzed by NS-MCM-41-Pd to produce ynones and ketones
碩士 === 國立臺北科技大學 === 有機高分子研究所 === 96 === Chemists have demonstrated the organic synthesis in a variety of palladium complex as a homogeneous catalyst which in contrast to heterogeneous catalyst, often difficult to be separated from the reaction mixtures. Nanosized mesoporous silica, NS-MCM-41, is a u...
Main Authors: | Jun-You Chen, 陳俊友 |
---|---|
Other Authors: | 蔡福裕 |
Format: | Others |
Language: | zh-TW |
Published: |
2008
|
Online Access: | http://ndltd.ncl.edu.tw/handle/323632 |
Similar Items
-
Acylation of Organozinc Reagents Catalyzed by Recyclable NS-MCM-41-Pd
by: Tze-Chiao Lin, et al.
Published: (2009) -
Borylation and Suzuki Reaction Catalyzed by NS-MCM-41-Pd and its One-Pot Application
by: Chun-Chin Chou, et al.
Published: (2007) -
Substrate-Controlled Product Divergence: Silver-Catalyzed Reaction of Trifluoromethyl Ketones with Terminal Alkynes
by: Fang-Ling Li, et al.
Published: (2017-03-01) -
Sonogashira Reaction of Aryl and Heteroaryl Halides with Terminal Alkynes Catalyzed by a Highly Efficient and Recyclable Nanosized MCM-41 Anchored Palladium Bipyridyl Complex
by: Chung-Yuan Mou, et al.
Published: (2010-12-01) -
Highly efficient transition metal-free coupling of acid chlorides with terminal alkynes in [bmim]Br: A rapid route to access ynones using MgCl2
by: Mohammad Navid Soltani Rad
Published: (2018-03-01)