@article { ISI:000302023500063, title = {Efficient, rapid synthesis of bis(indolyl)methane using ethyl ammonium nitrate as an ionic liquid}, journal = {RSC Advances}, volume = {2}, number = {8}, year = {2012}, month = {MAR}, pages = {3525-3529}, publisher = {ROYAL SOC CHEMISTRY}, type = {Article}, address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND}, abstract = {

A simple and rapid protocol has been developed for an efficient synthesis of bis( indolyl)methane in excellent yields using ethyl ammonium nitrate (EAN) as reusable ionic liquid at room temperature. The protocol involves an electrophilic substitution reaction of indoles with several aldehydes.

}, issn = {2046-2069}, doi = {10.1039/c2ra00849a}, author = {Mulla, Shafeek Abdul Rashid and Sudalai, A. and Pathan, Mohsinkhan Y. and Siddique, Shafi A. and Inamdar, Suleman M. and Chavan, Santosh S. and Reddy, R. Santosh} } @article { ISI:000341552000026, title = {Efficient synthesis of O-aryloxime ethers by copper fiuorapatite catalyzed cross-coupling of aryloximes with arylboronic acids}, journal = {Tetrahedron Letters}, volume = {55}, number = {38}, year = {2014}, month = {SEP}, pages = {5327-5332}, publisher = {PERGAMON-ELSEVIER SCIENCE LTD}, type = {Article}, address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND}, abstract = {

A novel, highly efficient, and mild protocol has been developed for the synthesis of O-aryloxime ethers in good to excellent yields at ambient reaction conditions. This is the first report in which =N-O-Ar linkage was achieved with ecofriendly, recyclable, heterogeneous copper fluorapatite (CuFAP) catalyst via C-O cross coupling of aryloxime with arylboronic acid in the presence of Cs2CO3 as base and methanol as solvent. (C) 2014 Elsevier Ltd. All rights reserved.

}, keywords = {Arylboronic acid, Aryloxime, Copper fluorapatite, O-Aryloxime ethers}, issn = {0040-4039}, doi = {10.1016/j.tetlet.2014.07.056}, author = {Mulla, Shafeek Abdul Rashid and Chavan, Santosh S. and Inamdar, Suleman M. and Pathari, Mohsinkhan Y. and Shaikh, Taufeekaslam M. Y.} } @article { ISI:000358349700002, title = {Enantioselective cooperative catalysis}, journal = {Organic \& Biomolecular Chemistry}, volume = {13}, number = {30}, year = {2015}, month = {JUN}, pages = {8116-8162}, publisher = {ROYAL SOC CHEMISTRY}, address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND}, abstract = {

In recent years, enantioselective cooperative catalytic reactions, wherein two catalysts work simultaneously to form products which cannot be obtained by the use of a single catalyst alone, have attracted considerable attention. This review focuses on this emerging field, with particular emphasis on mechanistic aspects, which will help readers to understand the role of each catalyst.

}, issn = {1477-0520}, doi = {10.1039/c5ob00986c}, author = {Inamdar, Suleman M. and Shinde, Valmik S. and Patil, Nitin T.} } @article { ISI:000364449200020, title = {Engineering ligands on the Au center: discovering broadly applicable gold catalysis with high turnover numbers}, journal = {Organic Chemistry Frontiers}, volume = {2}, number = {8}, year = {2015}, month = {JUN}, pages = {995-998}, publisher = {CHINESE CHEMICAL SOC}, address = {PO BOX 1-18, NANKANG, TAIPEI 115, TAIWAN}, abstract = {

The research groups of Hammond/Xu and Zhang report the discovery of new ligands for gold catalysis. With these ligands, gold catalyzed reactions have been reported for a broader range of substrates with very high TONs at a level that can match the needs of large-scale applications.

}, issn = {2052-4129}, doi = {10.1039/c5qo00162e}, author = {Inamdar, Suleman M. and Patil, Nitin T.} }