Chemoselective reduction and transesterification of α-keto propargylic esters mediated by NaBH < inf > 4 < /inf > and CeCl < inf > 3 < /inf > 7H < inf > 2 < /inf > O
Chemoselective reduction and transesterification of α-keto propargylic esters mediated by NaBH < inf > 4 < /inf > and CeCl < inf > 3 < /inf > 7H < inf > 2 < /inf > O
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Date
2011-01-01
Authors
Saravanan, Thangavel
Chadha, Anju
Journal Title
Journal ISSN
Volume Title
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Abstract
An efficient one-pot synthesis of α-hydroxy propargylic esters by chemoselective reduction followed by transesterification using NaBH4 in combination with CeCl37H2O is described. © 2011 Taylor & Francis Group, LLC.
Description
Keywords
NaBH /CeCl 7H O 4 3 2,
reduction,
transesterification
Citation
Synthetic Communications. v.41(16)