@article { ISI:000243272400038, title = {BINOL: a versatile chiral reagent}, journal = {Synlett}, number = {19}, year = {2006}, month = {DEC}, pages = {3366-3367}, publisher = {GEORG THIEME VERLAG KG}, type = {Article}, address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY}, issn = {0936-5214}, doi = {10.1055/s-2006-956459}, author = {Pandey, Satyendra Kumar} } @article { ISI:000238111400016, title = {Enantioselective synthesis of (2R,3R)- and (2S,3S)-beta-hydroxyornithine}, journal = {Tetrahedron Letters}, volume = {47}, number = {25}, year = {2006}, month = {JUN}, pages = {4167-4169}, publisher = {PERGAMON-ELSEVIER SCIENCE LTD}, type = {Article}, address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND}, abstract = {

An efficient and short synthesis of (2R,3R)- and (2S,3S)-beta-hydroxyornithine 1a-b is described using Sharpless asymmetric dihydroxylation and regioselective nucleophilic opening of a cyclic sulfite as the key steps. (c) 2006 Elsevier Ltd. All rights reserved.

}, issn = {0040-4039}, doi = {10.1016/j.tetlet.2006.04.055}, author = {Pandey, Satyendra Kumar and Kumar, Pradeep} } @article { ISI:000251507000029, title = {Concise synthesis of (-)-deoxoprosopinine}, journal = {Synlett}, number = {18}, year = {2007}, month = {NOV}, pages = {2894-2896}, publisher = {GEORG THIEME VERLAG KG}, type = {Article}, address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY}, abstract = {

A simple and highly efficient approach to (-)-deoxoprosopinine from racemic epoxide as a starting material is described employing a Jacobsen{\textquoteright}s hydrolytic kinetic resolution (HKR) and Sharpless asymmetric dihydroxylation (AD) as key steps.

}, keywords = {hydroboration-oxidation, Jacobsen{\textquoteright}s HKR, Piperidine alkaloids, sharpless AD, Total synthesis}, issn = {0936-5214}, doi = {10.1055/s-2007-991056}, author = {Pandey, Satyendra Kumar and Kumar, Pradeep} } @article { ISI:000243519300018, title = {Efficient total synthesis of (-)-(3S,6R)-3,6-dihydroxy-10-methylundecanoic acid}, journal = {European Journal of Organic Chemistry}, number = {2}, year = {2007}, month = {JAN}, pages = {369-373}, publisher = {WILEY-V C H VERLAG GMBH}, type = {Article}, address = {PO BOX 10 11 61, D-69451 WEINHEIM, GERMANY}, abstract = {

An efficient enantioselective synthesis of (-)-(3S,6R)-3,6-dihydroxy-10-methylundecanoic acid (1) from epichlorohydrin is described. The key steps include Jacobsen{\textquoteright}s HKR, Sharpless asymmetric dihydroxylation, regioselective opening of epoxide and cyclic sulfate. ((c) Wiley-VCH Verlag GmbH \& Co. KGaA, 69451 Weinheim, Germany, 2007).

}, keywords = {cyclic sulfate, Dihydroxylation, Grignard reaction, hydroboration-oxidation, Jacobsen{\textquoteright}s hydrolytic kinetic resolution (HKR), regio selectivity}, issn = {1434-193X}, doi = {10.1002/ejoc.200600690}, author = {Pandey, Satyendra Kumar and Kumar, Pradeep} } @article { ISI:000255827100025, title = {Concise synthesis of protected (2S,4R)-4-hydroxyornithine}, journal = {Tetrahedron Letters}, volume = {49}, number = {20}, year = {2008}, month = {MAY}, pages = {3297-3299}, publisher = {PERGAMON-ELSEVIER SCIENCE LTD}, type = {Article}, address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND}, abstract = {

A short synthesis of the nonproteinogenic amino acid, (2S,4R)-4-hydroxyornithine is described. Starting from racemic benzyl glycidol, the scaffold of the target compound was constructed in high enantio- and diastereoselectivity using Jacobsen{\textquoteright}s hydrolytic kinetic resolution (HKR) and regioselective opening of an epoxide as key steps. (c) 2008 Elsevier Ltd. All rights reserved.

}, keywords = {Epoxide, Grignard reaction, hydroxyornithine, Jacobsen{\textquoteright}s HKR, Natural product}, issn = {0040-4039}, doi = {10.1016/j.tetlet.2008.03.076}, author = {Pandey, Satyendra Kumar and Pandey, Menaka and Kumar, Pradeep} } @article { ISI:000264471400009, title = {General approach to medium-sized ring ethers via hydrolytic and oxidative kinetic resolutions: stereoselective syntheses of (-)-cis-lauthisan and (+)-isolaurepan}, journal = {Tetrahedron}, volume = {65}, number = {11}, year = {2009}, month = {MAR}, pages = {2226-2231}, publisher = {PERGAMON-ELSEVIER SCIENCE LTD}, address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND}, abstract = {

A short and enantioselective approach to medium ring ethers and its application to the syntheses of (-)-cis-lauthisan and (+)-isolaurepan are described. The synthetic strategy features Jacobson{\textquoteright}s Hydrolytic Kinetic Resolution (HKR), oxidative resolution of secondary alcohol, and highly diastereoselective Et(3)SiH/TMSOTf-promoted reductive cyclization of a hydroxy ketone to give exclusively the different medium-sized cis-disubstituted cyclic ethers. (C) 2009 Elsevier Ltd. All rights reserved.

}, keywords = {cis-Reductive cyclization, Jacobson{\textquoteright}s Hydrolytic Kinetic Resolution (HKR), Oxepanes, Oxidative resolution of secondary alcohol, Ring ether}, issn = {0040-4020}, doi = {10.1016/j.tet.2009.01.062}, author = {Tripathi, Divya and Pandey, Satyendra Kumar and Kumar, Pradeep} }