Record Details

Selected synthetic strategies to spirocyclics

DSpace at IIT Bombay

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Field Value
 
Title Selected synthetic strategies to spirocyclics
 
Creator KOTHA, S
DEB, AC
LAHIRI, K
MANIVANNAN, E
 
Subject spiro compounds
metathesis
diels-alder reactions
domino reactions
suzuki coupling
radical reactions
ring closure
ring-closing metathesis
cyclic 1-amino-1-carboxylic acids
carbocyclic spiro compounds
asymmetric total-synthesis
quaternary carbon centers
formal total-synthesis
diels-alder reaction
fredericamycin-a
claisen rearrangement
stereoselective construction
 
Description The design and synthesis of spirocycles is a challenging task because it involves the creation of a quaternary center, which itself is considered to be one of the most difficult tasks among synthetic transformations. Some recent approaches based on metathesis, cycloaddition and transition-metal-mediated transformations to spirocycles are described here.
 
Publisher GEORG THIEME VERLAG KG
 
Date 2011-10-13T20:48:30Z
2011-12-15T09:16:13Z
2011-10-13T20:48:30Z
2011-12-15T09:16:13Z
2009
 
Type Review
 
Identifier SYNTHESIS-STUTTGART,(2)165-+
0039-7881
http://dx.doi.org/10.1055/s-0028-1083300
http://dspace.library.iitb.ac.in/xmlui/handle/10054/13846
http://hdl.handle.net/100/3054
 
Language en