Saket B. Bhagat
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Saket B. Bhagat has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
Vikas N. Telvekar
Department of Pharmaceutical Sciences & Technology, Institute of Chemical Technology
4 shared publications- Vikas N. Telvekar
Department of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Mumbai, 400019, India
2 shared publications - Yogesh B. Sutar
Department of Pharmaceutical Sciences, The Daniel K. Inouye College of Pharmacy, University of Hawaii Hilo, Hilo, HI 96720, USA
2 shared publications Harshal M. Bachhav
1 shared publication- Shrikant M. Ghodse
Principal K.M. Kundnani College of Pharmacy, Mumbai, India
1 shared publication Yogesh Manohar
1 shared publication
Latest Publications
- 7 February 2018
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 29 (07) , 874-879
l-Proline: An Efficient Organocatalyst for the Synthesis of 5-Substituted 1H-Tetrazoles via [3+2] Cycloaddition of Nitriles and Sodium Azide
A simple and efficient route for the synthesis of a series of 5-substituted 1H-tetrazoles using l-proline as a catalyst from structurally diverse organic nitriles and sodium azide is reported. The prominent features of this environmentally benign, cost effective, and high-yielding l-proline-catalyzed protocol includes simple experimental procedure, short reaction time, simple workup, and excellent yields making it a safer and economical alternative to hazardous Lewis acid catalyzed methods. The protocol was successfully applied to a broad range of substrates, including aliphatic and aryl nitriles, organic thiocyanates, and cyanamides.
- 7 February 2018
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 29 (07) , 874-879
l-Proline: An Efficient Organocatalyst for the Synthesis of 5-Substituted 1H-Tetrazoles via [3+2] Cycloaddition of Nitriles and Sodium Azide
A simple and efficient route for the synthesis of a series of 5-substituted 1H-tetrazoles using l-proline as a catalyst from structurally diverse organic nitriles and sodium azide is reported. The prominent features of this environmentally benign, cost effective, and high-yielding l-proline-catalyzed protocol includes simple experimental procedure, short reaction time, simple workup, and excellent yields making it a safer and economical alternative to hazardous Lewis acid catalyzed methods. The protocol was successfully applied to a broad range of substrates, including aliphatic and aryl nitriles, organic thiocyanates, and cyanamides.
- 1 September 2017
- Published by Elsevier in Tetrahedron Letters
- Vol. 58 (37) , 3662-3666
NBS mediated protocol for the synthesis of N -bridged fused heterocycles in water
- 1 September 2017
- Published by Elsevier in Tetrahedron Letters
- Vol. 58 (37) , 3662-3666
NBS mediated protocol for the synthesis of N -bridged fused heterocycles in water
- 1 December 2015
- Published by Elsevier in Tetrahedron Letters
- Vol. 56 (48) , 6768-6771
General and efficient oxidative amidation of benzyl alcohols with amines using diacetoxyiodobenzene and TBHP
- 1 December 2015
- Published by Elsevier in Tetrahedron Letters
- Vol. 56 (48) , 6768-6771
General and efficient oxidative amidation of benzyl alcohols with amines using diacetoxyiodobenzene and TBHP
- 1 October 2011
- Published by Elsevier in Tetrahedron Letters
- Vol. 52 (43) , 5697-5701
Efficient protocol for the synthesis of quinoxaline, benzoxazole and benzimidazole derivatives using glycerol as green solvent
- 1 October 2011
- Published by Elsevier in Tetrahedron Letters
- Vol. 52 (43) , 5697-5701
Efficient protocol for the synthesis of quinoxaline, benzoxazole and benzimidazole derivatives using glycerol as green solvent