Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/6227
Title: Stereoretentive Chlorination of Cyclic Alcohols Catalyzed by Titanium(IV) Tetrachloride: Evidence for a Front Side Attack Mechanism
Authors: Deboprosad, Mondal
Song Ye, Li
Luca, Bellucci
Teodoro, Laino
Tafi, Andrea 
Salvatore, Guccione
Salvatore D., Lepore
Issue Date: 2013
Project: None 
Journal: JOURNAL OF ORGANIC CHEMISTRY
Abstract: 
A mild chlorination reaction of alcohols was developed using the classical thionyl chloride reagent but with added catalytic titanium(IV) chloride. These reactions proceeded rapidly to afford chlorination products in excellent yields and with preference for retention of configuration. Stereoselectivities were high for a variety of chiral cyclic secondary substrates including sterically hindered systems. Chlorosulfites were first generated in situ and converted to alkyl chlorides by the action of titanium tetrachloride which is thought to chelate the chlorosulfite leaving group and deliver the halogen nucleophile from the front face. To better understand this novel reaction pathway, an ab initio study was undertaken at the DFT level of theory using two different computational approaches. This computational evidence suggests that while the reaction proceeds through a carbocation intermediate, this charged species likely retains pyramidal geometry existing as a conformational isomer stabilized through hyperconjugation (hyperconjomers). These carbocations are then essentially “frozen” in their original configurations at the time of nucleophilic capture.
Description: 
58802
URI: http://hdl.handle.net/20.500.12779/6227
ISSN: 0022-3263
DOI: 10.1021/jo3023439
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