@article { ISI:000233784100018, title = {Asymmetric aminohydroxylation route to (+)-L-733,060}, journal = {Tetrahedron-Asymmetry}, volume = {16}, number = {21}, year = {2005}, month = {OCT}, pages = {3579-3583}, publisher = {PERGAMON-ELSEVIER SCIENCE LTD}, type = {Article}, address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND}, abstract = {

An enantioselective synthesis of (+)-L-733,060 starting from cinnamic acid using Sharpless asymmetric aminohydroxylation and Wittig reactions as the key steps is described. (c) 2005 Elsevier Ltd. All rights reserved.

}, issn = {0957-4166}, doi = {10.1016/j.tetasy.2005.09.010}, author = {Kandula, Subba Rao V. and Kumar, Pradeep} } @article { ISI:000232860200017, title = {Asymmetric synthesis of (-)-alpha-conhydrine}, journal = {Tetrahedron-Asymmetry}, volume = {16}, number = {19}, year = {2005}, month = {OCT}, pages = {3268-3274}, publisher = {PERGAMON-ELSEVIER SCIENCE LTD}, type = {Article}, address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND}, abstract = {

The enantioselective synthesis of (-)-alpha-conhydrine has been achieved by two different synthetic routes. The key steps include Sharpless asymmetric dihydroxylation, regioselective opening of a cyclic sulfate and Wittig olefination. (c) 2005 Elsevier Ltd. All rights reserved.

}, issn = {0957-4166}, doi = {10.1016/j.tetasy.2005.08.045}, author = {Kandula, Subba Rao V. and Kumar, Pradeep} } @article { ISI:000241064000015, title = {Asymmetric aminohydroxylation route to cis-2,6-disubstituted piperidine-3-ol: application to the synthesis of (-)-deoxocassine}, journal = {Tetrahedron}, volume = {62}, number = {42}, year = {2006}, month = {OCT}, pages = {9942-9948}, publisher = {PERGAMON-ELSEVIER SCIENCE LTD}, type = {Article}, address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND}, abstract = {

A highly efficient, flexible, and convergent route to cis-2,3,6-trisubstituted piperidines has been developed employing the Sharpless asymmetric aminohydroxylation and stereoselective reductive amination by catalytic hydrogenation as the key steps. Its usage is illustrated by the short synthesis of the piperidine-3-ol alkaloid, (-)-deoxocassine. (c) 2006 Elsevier Ltd. All rights reserved.

}, issn = {0040-4020}, doi = {10.1016/j.tet.2006.08.014}, author = {Kandula, Subba Rao V. and Kumar, Pradeep} }