Organocatalytic domino double Michael and the subsequent radical cyclization or Pictet-Spengler reaction
碩士 === 國立中正大學 === 化學暨生物化學研究所 === 100 === Asymmetric synthesis of highly functionalized compounds were achieved by a sequential organocatalyzed double Michael reaction of conjugated esters and α,β - unsaturated aldehydes, and radical cyclization or Pictet-Spengler reaction with high enantioselectivit...
Main Authors: | Liao, Wei-Kai, 廖威凱 |
---|---|
Other Authors: | Hong, Bor-Cherng |
Format: | Others |
Language: | zh-TW |
Published: |
2012
|
Online Access: | http://ndltd.ncl.edu.tw/handle/39872207087389884966 |
Similar Items
-
Organocatalytic Synthesis of Functionalized Cyclohexanes via Domino Michael/Michael/Cyclization Reaction
by: 簡崇瀚
Published: (2013) -
The Pictet-Spengler Reaction Updates Its Habits
by: Andrea Calcaterra, et al.
Published: (2020-01-01) -
Heterogeneous Catalysts in Pictet-Spengler-Type Reactions
by: Rodolfo Quevedo, et al.
Published: (2013-01-01) -
Elaboration of the Isochromane System of Stephaoxocanes Employing an Oxa-Pictet Spengler Type Cyclization
by: Carmem R. Bernardi, et al.
Published: (2000-03-01) -
Catalytic Enantioselective Approaches to the oxa-Pictet–Spengler Cyclization and Other 3,6-Dihydropyran-Forming Reactions
by: Zhengbo Zhu, et al.
Published: (2019-07-01)