@article { ISI:000229476800007, title = {Facile oxidation of flavanones to flavones using [hydroxy(tosyloxy)iodo]benzene in an ionic liquid}, journal = {Mendeleev Communications}, volume = {15}, number = {3}, year = {2005}, month = {MAY}, pages = {100-101}, publisher = {ELSEVIER SCIENCE BV}, type = {Article}, address = {PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS}, abstract = {

A method for the oxidation of flavationes to flavones has been developed using [hydroxy(tosyloxy)iodo] benzene (HTIB) in the room-temperature ionic liquid 1,3-di-n-butylimidazolium bromide ([bbim]Br-+(-)).

}, issn = {0959-9436}, doi = {10.1070/MC2005v015n03ABEH001997}, author = {Muthukrishnan, Murugan and Patil, P. S. and More, Shivaji V. and Joshi, Ramesh A.} } @article { ISI:000265958900008, title = {First ionic liquid-promoted Kabbe condensation reaction for an expeditious synthesis of privileged bis-spirochromanone scaffolds}, journal = {Tetrahedron Letters}, volume = {50}, number = {22}, year = {2009}, month = {JUN}, pages = {2643-2648}, publisher = {PERGAMON-ELSEVIER SCIENCE LTD}, address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND}, abstract = {

A variety of privileged bis-spirochromanones were synthesized for the First time from 4,6-diacetyl resorcinol in one-pot by carrying out the Kabbe condensation in loom temperature ionic liquid [bbim]Br. (C) 2009 Elsevier Ltd. All rights reserved.

}, keywords = {Bis-spirochromanone, Ionic liquid, Kabbe condensation, Morpholine}, issn = {0040-4039}, doi = {10.1016/j.tetlet.2009.03.104}, author = {Muthukrishnan, Murugan and Basavanag, U. M. V. and Puranik, Vedavati G.} } @article { ISI:000286862600011, title = {Facile enantioselective synthesis of enantiomerically pure (R)-phenoxybenzamine hydrochloride using the hydrolytic kinetic resolution method}, journal = {Tetrahedron-Asymmetry}, volume = {21}, number = {23}, year = {2010}, month = {DEC}, pages = {2825-2829}, publisher = {PERGAMON-ELSEVIER SCIENCE LTD}, address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND}, abstract = {

A practical and highly efficient enantioselective synthesis of (R)-phenoxybenzamine hydrochloride has been described for the first time using Jacobsen{\textquoteright}s hydrolytic kinetic resolution of a terminal epoxide as a key step and source of chirality. (C) 2010 Elsevier Ltd. All rights reserved.

}, issn = {0957-4166}, doi = {10.1016/j.tetasy.2010.11.011}, author = {Nikalje, Milind D. and Sasikumar, Murugesan and Muthukrishnan, Murugan} } @article { ISI:000295444000015, title = {First asymmetric synthesis of the antiepileptic drug lacosamide (Vimpat (R)) based on a hydrolytic kinetic resolution strategy}, journal = {Tetrahedron-Asymmetry}, volume = {22}, number = {12}, year = {2011}, month = {JUN}, pages = {1353-1357}, publisher = {PERGAMON-ELSEVIER SCIENCE LTD}, address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND}, abstract = {

An efficient asymmetric synthesis of the new antiepileptic drug, Lacosamide is described in high enantiopurity (\>98\% ee), using Jacobsen{\textquoteright}s hydrolytic kinetic resolution strategy as a key step. (C) 2011 Elsevier Ltd. All rights reserved.

}, issn = {0957-4166}, doi = {10.1016/j.tetasy.2011.07.024}, author = {Muthukrishnan, Murugan and Mujahid, Mohammad and Sasikumar, M. and Mujumdar, P.} }