Ministry of Education
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Dr Vijaya Anand Ramasamy

vidwan id: 48265
Male

Professor, Department of Chemical Sciences
Indian Institute of Science Education and Research(IISER), Mohali

Orchid Icon 0000-0001-9490-4569 Google Scholar Icon 35081351400 Google Scholar Icon Fpz56JkAAAAJ&hl

Expertise

  • Organic Chemistry

Publications

Total Articles 83
Books 0
Proceedings 0

Publications

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Scopus

Citations 1249
h-index 21

CrossRef

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Citations 949
h-index 18
Google Scholar

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Professional Recognition

2022

CRSI Bronze Medal

Chemical Research Society of India (CRSI)

Community & Membership

2021

Resonance Journal

Associate Editor
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Bio

My research group is focusing on the following areas: 1. Organocatalyzed enantioselective transformations using chiral N-heterocyclic carbene (NHC) as a catalyst 2. Development of a new class of chiral NHC-metal complexes and their applications in CH activation chemistry 3. Total synthesis of natural and unnatural biologically active complex molecules 4. Synthesis of unnatural small peptides and their applications in organocatalysis.

Personal Details

  • Male
  • Professor , Indian Institute of Science Education and Research(IISER), Mohali
  • IISER Mohali
Ph.D
Other Institute 2003
Professor Nov 2022 – Present
Indian Institute of Science Education and Research(IISER), Mohali | Department of Chemical Sciences

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Co-Authors (3)

Khagga

Dr Khagga Mukkanti

Jawaharlal Nehru Technological University Hyderabad

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Prof S. S. V. Rama Sastry

Indian Institute of Science Education and Research(IISER), Mohali

Ruchi

Dr Ruchi Anand

Indian Institute of Technology Bombay

Scholarly Work

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Scholarly Publications

Synthesis of related substances of olmesartan medoxomil, antihypertensive drug

Open Access
Article
Arkivoc. Year: 2010. Volume: 2010 , Issue: 2 , Pages: 292-302 .
Authors: Babu K.S.;Tagore A.R.;Reddy G.S.;Venkateswarlu G.;Reddy P.P.;Anand R.V.
DOI 10.3998/ark.5550190.0011.224
8 11

Efficient synthesis of olmesartan medoxomil, an antihypertensive drug

Open Access
Article
Synthetic Communications. Year: 2009. Volume: 39 , Issue: 2 , Pages: 291-298 .
Authors: Babu K.S.;Reddy M.S.;Tagore A.R.;Reddy G.S.;Sebastian S.;Varma M.S.;Venkateswarlu G.;Bhattacharya A.;Reddy P.P.;Anand R.V.
DOI 10.1080/00397910802372558
15 24

Expeditious synthesis of ramipril: An angiotensin converting enzyme (ACE) inhibitor

Open Access
Article
Synthetic Communications. Year: 2008. Volume: 38 , Issue: 11 , Pages: 1737-1744 .
Authors: Malakondaiah G.C.;Gurav V.M.;Reddy L.A.;Babu K.S.;Bhaskar B.V.;Reddy P.P.;Bhattacharya A.;Anand R.V.
DOI 10.1080/00397910801989238
8 6

Boric acid: an efficient and environmentally benign catalyst for transesterification of ethyl acetoacetate

Open Access
Article
Tetrahedron Letters. Year: 2008. Volume: 49 , Issue: 1 , Pages: 106-109 .
Authors: Kondaiah G.;Reddy L.;Babu K.;Gurav V.;Huge K.;Bandichhor R.;Reddy P.;Bhattacharya A.;Anand R.
DOI 10.1016/j.tetlet.2007.11.008
51 67

An investigation on key parameters that influence the resolution of omeprazole sodium

Open Access
Article
Year: 2008. Volume: 12 , Issue: 1 , Pages: 66-68 .
Authors: Reddy L.A.;Malakondaiah G.C.;Babu K.S.;Bhattacharya A.;Bandichhor R.;Himabindu V.;Reddy P.P.;Anand R.V.
DOI 10.1021/op700151c
2 3

Effect of solvent on stereoselectivity in Pd/C (Type 39K)-catalyzed hydrogenation of methyl 3-oxo-4-aza-5-androstene-17-carboxylate, a key intermediate for finasteride and dutasteride

Open Access
Article
Year: 2007. Volume: 11 , Issue: 5 , Pages: 889-891 .
Authors: Karrothu S.B.;Kolla N.;Lekkala A.R.;Golla C.M.;Anand R.V.;Gandu V.;Bhattacharya A.;Padi P.R.;Bandichhor R.
DOI 10.1021/op700104f
6 8

A ring-closing metathesis approach toward formal total synthesis of (+)-diplodialide A

Open Access
Article
Year: 2003. Volume: 68 , Issue: 8 , Pages: 3356-3359 .
Authors: Anand R.V.;Baktharaman S.;Singh V.K.
15 28

Silica gel induced cleavage of aziridines by aromatic amines under solvent free conditions

Open Access
Article
Tetrahedron Letters. Year: 2002. Volume: 43 , Issue: 22 , Pages: 3975-3976 .
Authors: Anand R.V.;Pandey G.;Singh V.K.
DOI 10.1016/S0040-4039(02)00727-X
40 44