Research Group Publications

 
  • R. C. Jagdhane, M. T. Patil, S. Krishnaswamy And M. S. Shashidhar, The orientation of the ?-hydroxyl group controls the diastereoselectivity during the hydride reduction and Grignard reaction of inososes, Tetrahedron., 69, 5144 - 5151 (2013).
  • M. I. Tamboli, S. Krishnaswamy, R. G. Gonnade And M. S. Shashidhar, Identification of molecular crystals capable of undergoing acyl-transfer reaction based on intermolecular interactions in the crystal lattice, Chem. Eur. J., 19, 12867 - 12874 (2013).
  • B. P. Gurale, M. S. Shashidhar And R. G. Gonnade, Synthesis of the aminocyclitol units of (–) hygromycin A and methoxyhygromycin from myo-inositol, J. Org. Chem., 77, 5801 - 5807 (2012).
  • K. Manoj, R. G. Gonnade, M. S. Shashidhar And M. M. Bhadbhade, Solvent induced crystallization of 1,2,3,4(6),5-penta-O-acetyl-6(4)-O-[(1S)-10-camphor sulphonyl]-myo-inositol diastereomers associated via weak trifurcated C-H?O interactions, Cryst Eng Comm. ., 14, 1716 - 1722 (2012).
  • B. P. Gurale, K. Vanka And M. S. Shashidhar., Radical mediated deoxygenation of inositol benzylidene acetals: Conformational analysis, DFT calculations and mechanism. , Carbohydr Res., 351, 26 - 3 (2012).
  • B. P. Gurale, R. G. Gonnade And M. S. Shashidhar., Chiral cryastals from an achiral molecule: 4,6-di-O-benzyl-1,3-O-benzylidene-2-O-(4-methoxybenzyl)-myo-5-inosose. , Acta cryst. C., C68, o183 - o187 (2012).
  • B. P. Gurale, M. S. Shashidhar And R. G. Gonnade, Synthesis of the Aminocyclitol units of (-)-Hygromycin A and Methoxyhygromycin from myo-inositol, J.Org. Chem., 77, 5801 - 5807 (2012).
  • R. S. Sardessai, S. Krishnaswami And M. S. Shashidhar, Achieving molecular stability of racemic 4-O-benzyl-myo-inositol-1,3,5-orthoformate through crystal formation. , Cryst Eng Comm., 14, (2012).
  • S. Krishnaswami, M. S. Shashidhar And M. M. Bhadbhade, Intermolecular benzoyl group transfer reactivity in crystals of racemic 2,6- di-O-benzoyl myo -inositol-1,3,5-orthobenzoate: controlling reactivity by solvate (pseudopolymorph) formation. , Cryst Eng Comm., 13, 3258 - 3264 (2011).
  • M. T. Patil, S. Krishnaswami, M. Sarmah And M. S. Shashidhar. , Protecting group directed stereoselective rduction of an epi-inosose: efficient synthesis of an epi inositol, Tetrahedron Lett., 52, 3756 - 3758 (2011).
  • B. P. Gurale, S. Krishnaswami, K. Vanka And M. S. Shashidhar, Thermal epimerization of inositol 1,3-benzylidene acetals in molten state. , Tetrahedron., 67, 7280 - 7288 (2011).
  • R. C. Jagdhane And M. S. Shashidhar., A Formal Synthesis of Valiolamine from myo-inositol, Tetrahedron., 67, 7963 - 7970 (2011).
  • M. T. Patil, M. S. Shashidhar And S. Krishnaswami, Comparisson of the crystal structures of racemic epi-inosose and (-)-epi-inosose. , Acta Cryst. C., C67, o435 - o438 (2011).
  • C. Murali, B. P. Gurale And M. S. Shashidhar, Intramolecular hydrogen abstraction in radicals derived from Inositol 1,3-acetals: efficient access to cyclitols. , Eur. J. Org. Chem., , 755 - 764 (2010).
  • R. C. Jagdhane And M. S. Shashidhar, Orthogonally protected cyclohexane hexols by ?one reaction ? one product? approach: efficient access to cyclitols and their derivatives, Eur. J. Org. Chem., , 2945 - 2953 (2010).
  • K. Manoj, R. G. Gonnade, M. M. Bhadbhade And M. S. Shashidar, Conformational polymorphism in racemic 2,4-di-O-benzoyl-6-O-tosyl myo-inositol 1,3,5-orthoacetate. , J. Str. Chem., 51, C 725 - 730 (2010).
  • S. Krishnaswami, R. G. Gonnade, M. S. Shashidhar And M. M. Bhadbhade. , Solvent induced helical assembly of molecules linked via O-H???O hydrogen bonding in solvatomorphs of racemic 2,6-di-O-(p-halobenzoyl)-myo-inositol 1,3,5-orthoformates. , Cryst Eng Comm., 12, 4184 - 4197 (2010).
  • K. Manoj, R. G. Gonnade, M. M. Bhadbhade And M. S. Shashidhar, Dipolar S=O...C=O and C-H...O interactions in the molecular organization of 2-O-tosyl-4,6-di-O-acetyl-myo-inositol 1,3,5-orthoesters, Acta Cryst., C65, o335 - O338 (2009).
  • M. T. Patil And M. S. Shashidhar. , Effect of protecting groups on reaction of inositol derivatives , Trends Carbohydr Res. In press., , (0000).