Vrushali H. Jadhav
Affiliations: | 2013- | CSIR-National Chemical Laboratory, Pune, India |
Area:
Synthetic carbohydrate chemistryWebsite:
http://academic.ncl.res.in/profile/vh.jadhavGoogle:
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Publications
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Thombal RS, Jadhav VH. (2016) Sulfonated graphene oxide as highly efficient catalyst for glycosylation Journal of Carbohydrate Chemistry. 35: 57-68 |
Jadhav VH, Bande OP, Puranik VG, et al. (2010) Synthesis of azepane and nojirimycin iminosugars: the Sharpless asymmetric epoxidation of d-glucose-derived allyl alcohol and highly regioselective epoxide ring opening using sodium azide Tetrahedron: Asymmetry. 21: 163-170 |
Jadhav VH, Bande OP, Puranik VG, et al. (2010) Synthesis of eight-membered iminocyclitols from d-glucose Tetrahedron. 66: 2830-2834 |
Jadhav VH, Bande OP, Pinjari RV, et al. (2009) Synthesis and conformational study of chiral oxepines: the Baylis-Hillman reaction and RCM approach with sugar aldehyde. The Journal of Organic Chemistry. 74: 6486-94 |
Dhavale D, Bande O, Jadhav V, et al. (2009) Highly Diastereoselective 1,3-Dipolar Cycloaddition of a d-Galactose-Derived Nitrone with Dimethyl Maleate: Synthesis of Polyhydroxylated PerhydroazaÂazulenes Synlett. 2009: 1959-1963 |
Bande OP, Jadhav VH, Puranik VG, et al. (2009) Stereo-controlled approach to pyrrolidine iminosugar C-glycosides and 1,4-dideoxy-1,4-imino-l-allitol using a d-mannose-derived cyclic nitrone Tetrahedron Letters. 50: 6906-6908 |
Jadhav VH, Kumar KSA, Chaudhari VD, et al. (2007) Facile Method for Trimethylsilylation of Alcohols using Hexamethyldisilazane and Ammonium Thiocyanate under Neutral Conditions Synthetic Communications. 37: 1363-1370 |
Bande OP, Jadhav VH, Puranik VG, et al. (2007) 1,3-Dipolar cycloaddition reaction of a d-galactose derived nitrone with allyl alcohol: synthesis of polyhydroxylated perhydroazaazulene alkaloids Tetrahedron: Asymmetry. 18: 1176-1182 |
Jadhav VH, Kumar KSA, Chaudhari VD, et al. (2007) Facile Method for Trimethylsilylation of Alcohols Using Hexamethyldisilazane and Ammonium Thiocyanate under Neutral Conditions. Cheminform. 38 |