Protecting-group-directed regio- and stereoselective oxymercuration–demercuration: Synthesis of piperidine alkaloids containing 1,2- and 1,3-amino alcohol units

Bugde, S.T.; Volvoikar, P.S.; Tilve, S.G.

dc.contributor.author	Bugde, S.T.
dc.contributor.author	Volvoikar, P.S.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2018-02-19T04:24:18Z
dc.date.available	2018-02-19T04:24:18Z
dc.date.issued	2018
dc.identifier.citation	Synthesis. 50(5); 2018; 1113-1122.	en_US
dc.identifier.uri	https://doi.org/10.1055/s-0036-1589523
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/5101
dc.description.abstract	An efficient synthesis of naturally occurring 1,2- and 1,3-amino alcohol unit containing 2-substituted piperidine alkaloids and their analogues has been developed from l-pipecolinic acid. The protocol describes the regio- and stereoselective oxymercuration–demercuration of 2-alkenyl piperidines based on protecting groups to give piperidine alkaloids as a key step.	en_US
dc.publisher	Thieme Verlag	en_US
dc.subject	Chemistry	en_US
dc.title	Protecting-group-directed regio- and stereoselective oxymercuration–demercuration: Synthesis of piperidine alkaloids containing 1,2- and 1,3-amino alcohol units	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y