Ministry of Education
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Dr Satyasheel Sharma

vidwan id: 132339
Male

Assistant Professor, Department of Natural Products
National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad

Orchid Icon 0000-0002-4983-1572 Google Scholar Icon 55491679600 Google Scholar Icon h-jidJYAAAAJ

Expertise

  • Organic Chemistry

Publications

Total Articles 57
Books 0
Proceedings 0

Publications

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Scopus

Citations 3343
h-index 35

CrossRef

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Citations 3195
h-index 35
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Community & Membership

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Bio

Transition metal catalyzed C-H activation reactions for the synthesis of anticancer agents; Design and construction of fluorine containing scaffolds of pharmaceutical importance via C-H Bond activation

Personal Details

  • Male
  • Assistant Professor , National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad
  • NIPER Ahmedabad, Opposite Air force Station, Palaj
Ph.D
University of Delhi 2011
Assistant Professor Jul 2017 – Present
National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad | Department of Natural Products

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Co-Authors (6)

Abhijeet

Dr Abhijeet Kate

National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad

Akshay

Dr Akshay Srivastava

National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad

Amit

Dr Amit Shard

National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad

Bijoy P

Dr Bijoy P Mathew

VIMALA COLLEGE, THRISSUR

Mahendra

Prof Mahendra Nath

University of Delhi

Siddheshwar

Dr Siddheshwar Chauthe

National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad

Scholarly Work

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Scholarly Publications

Mild Rh(III)-catalyzed C7-allylation of indolines with allylic carbonates

Open Access
Article
Year: 2015. Volume: 80 , Issue: 3 , Pages: 1818-1827 .
Authors: Park J.;Mishra N.K.;Sharma S.;Han S.;Shin Y.;Jeong T.;Oh J.S.;Kwak J.H.;Jung Y.H.;Kim I.S.
DOI 10.1021/jo502733q
78 80

Rhodium(III)-catalyzed selective C-H cyanation of indolines and indoles with an easily accessible cyano source

Open Access
Article
Year: 2015. Volume: 357 , Issue: 6 , Pages: 1293-1298 .
Authors: Mishra N.;Jeong T.;Sharma S.;Shin Y.;Han S.;Park J.;Oh J.;Kwak J.;Jung Y.;Kim I.
DOI 10.1002/adsc.201401152
94 92

Synthesis of N-Sulfonylamidated and Amidated Azobenzenes under Rhodium Catalysis

Open Access
Article
Year: 2015. Volume: 80 , Issue: 16 , Pages: 8026-8035 .
Authors: Han S.;Mishra N.K.;Sharma S.;Park J.;Choi M.;Lee S.Y.;Oh J.S.;Jung Y.H.;Kim I.S.
DOI 10.1021/acs.joc.5b01149
33 32

Rh(III)-catalyzed direct coupling of azobenzenes with α-diazo esters: Facile synthesis of cinnolin-3(2 H)-ones

Open Access
Article
Organic Letters. Year: 2015. Volume: 17 , Issue: 11 , Pages: 2852-2855 .
Authors: Sharma S.;Han S.H.;Han S.;Ji W.;Oh J.;Lee S.Y.;Oh J.S.;Jung Y.H.;Kim I.S.
DOI 10.1021/acs.orglett.5b01298
107 114

Direct and site-selective palladium-catalyzed c-7 acylation of indolines with aldehydes

Open Access
Article
Year: 2015. Volume: 357 , Issue: 2-3 , Pages: 594-600 .
Authors: Shin Y.;Sharma S.;Mishra N.K.;Han S.;Park J.;Oh H.;Ha J.;Yoo H.;Jung Y.H.;Kima I.S.
DOI 10.1002/adsc.201400942
63 64

Rhodium-catalyzed mild and selective C-H allylation of indolines and indoles with 4-vinyl-1,3-dioxolan-2-one: Facile access to indolic scaffolds with an allylic alcohol moiety

Open Access
Article
Tetrahedron. Year: 2015. Volume: 71 , Issue: 16 , Pages: 2435-2441 .
Authors: Sharma S.;Shin Y.;Mishra N.K.;Park J.;Han S.;Jeong T.;Oh Y.;Lee Y.;Choi M.;Kim I.S.
DOI 10.1016/j.tet.2015.02.052
50 49

Ru(II)-catalyzed selective C-H amination of xanthones and chromones with sulfonyl azides: Synthesis and anticancer evaluation

Open Access
Article
Year: 2014. Volume: 79 , Issue: 19 , Pages: 9262-9271 .
Authors: Shin Y.;Han S.;De U.;Park J.;Sharma S.;Mishra N.K.;Lee E.K.;Lee Y.;Kim H.S.;Kim I.S.
DOI 10.1021/jo501709f
61 60

Pd-catalyzed oxidative coupling of arene C-H bonds with benzylic ethers as acyl equivalents

Open Access
Article
Year: 2014. Volume: 79 , Issue: 1 , Pages: 275-284 .
Authors: Han S.;Sharma S.;Park J.;Kim M.;Shin Y.;Mishra N.K.;Bae J.J.;Kwak J.H.;Jung Y.H.;Kim I.S.
DOI 10.1021/jo4024304
50 61