Core structure-based design of Organocatalytic [3+2]-Cycloaddition reactions: highly efficient and Stereocontrolled Syntheses of 3,3′-Pyrrolidonyl Spirooxindoles
Extraordinary levels of stereocontrol were achieved in an efficient organocatalytic asymmetric [3+2]-cycloaddition reaction between an α-isothiocyanato imide and various methyleneindolinones. Simple precursors were used for the rapid construction of spirocyclic oxindole derivatives with high enantio...
Main Authors: | Barbas III, Carlos F., Tan, Bin, Zeng, Xiaofei, Leong, Wendy Wen Yi, Shi, Zugui, Zhong, Guofu |
---|---|
Other Authors: | School of Physical and Mathematical Sciences |
Format: | Journal Article |
Language: | English |
Published: |
2013
|
Online Access: | https://hdl.handle.net/10356/99531 http://hdl.handle.net/10220/12896 |
Similar Items
-
Organocatalytic asymmetric 1,3-dipolarand formal 1,3-dipolar cycloaddition reactions.
by: Wang, Fei
Published: (2014) -
Enantiopure bicyclic piperidinones: Stereocontrolled cycloadditions
by: Brewster, A, et al.
Published: (2005) -
Stereocontrolled syntheses of the nemorensic acids using 6-diazoheptane-2,5-dione in carbonyl ylide cycloadditions.
by: Hodgson, D, et al.
Published: (2004) -
Organocatalytic asymmetric mannich, formal [4+1] and [4+2] annulation reactions
by: Shi, Zugui
Published: (2012) -
Studies towards a stereocontrolled synthesis of the tricarboxylate core of the zaragozic acids-squalestatins by a cycloaddition-rearrangement strategy
by: Hodgson, D, et al.
Published: (2000)