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Srinivas Gangula
Observed name:
Gangula Srinivas
Institution:
Tianjin Economic-Technological Development Area
Observed institutions:
Jawaharlal Nehru Technological University, Hyderabad,
Tianjin Economic-Technological Development Area,
Dr. Reddy's Laboratories (India),
Osmania University
ORCID:
0000-0002-3765-6877
Observed ORCID:
0000-0002-3765-6877
OpenAlex ID:
A5022725636
Commercial-Scale Visible Light Trifluoromethylation of 2-Chlorothiophenol Using CF 3 I Gas
2022
·
Kaid C. Harper
, En-Xuan Zhang
, et al.
·
Organic Process Research & Development
·
39
PDF
Substrate Modification Approach to Achieve Efficient Resolution: Didesmethylcitalopram: A Key Intermediate for Escitalopram
2007
·
Chandrashekar R. Elati
, Naveenkumar Kolla
, et al.
·
Organic Process Research & Development
·
26
Investigation of a Kumada Cross Coupling Reaction for Large-Scale Production of (2S, 7R, E)-2-Isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-N,N,8-trimethylnon-4-enamide
2015
·
Srinivas Gangula
, Uday Kumar Neelam
, et al.
·
Organic Process Research & Development
·
20
An efficient synthesis of dexlansoprazole employing asymmetric oxidation strategy
2011
·
Manne Naga Raju
, Neelam Uday Kumar
, et al.
·
Tetrahedron Letters
·
18
An Improved Process for the Production of Lansoprazole: Investigation of Key Parameters That Influence the Water Content in Final API
2009
·
Srinivas Gangula
, Chandrasekhar R. Elati
, et al.
·
Organic Process Research & Development
·
17
An Alternative Approach to Achieve Enantiopure (3S)-4-Benzyl-3- (4-fluorophenyl)morpholin-2-one: A Key Intermediate of Aprepitant, an NK1 Receptor Antagonist
2007
·
Naveenkumar Kolla
, Chandrashekar R. Elati
, et al.
·
Organic Process Research & Development
·
15
A convergent approach to the synthesis of aprepitant: a potent human NK-1 receptor antagonist
2007
·
Chandrashekar R. Elati
, Naveenkumar Kolla
, et al.
·
Tetrahedron Letters
·
14
Application of Continuous Flow Micromixing Reactor Technology for Synthesis of Benzimidazole Drugs
2013
·
Gunupati Sharathchandra Reddy
, Narra Santosh Reddy
, et al.
·
Organic Process Research & Development
·
13
Synthesis, Optimization, and Large-Scale Preparation of the Low-Dose Central Nervous System-Penetrant BACE1 Inhibitor LY3202626 via a [3 + 2] Nitrone Cycloaddition
2020
·
Pablo Garcia-Losada
, Amy C. DeBaillie
, et al.
·
Organic Process Research & Development
·
12
Development of a Scalable Process for an IL-17A Inhibitor LY3509754: Part I: Synthesis of the Pyridazinyl Imidazolidinone Intermediate Enabled by Biocatalysis and CSTR Technologies
2025
·
Qiang Yang
, Yu Lu
, et al.
·
Organic Process Research & Development
·
10
Novel Synthesis of Fosphenytoin: Anti-Convulsant Prodrug
2008
·
Chandrashekar R. Elati
, Srinivas Gangula
, et al.
·
Synthetic Communications
·
10
Improved Process for Paroxetine Hydrochloride Substantially Free from Potential Impurities
2012
·
Srinivas Gangula
, Naveen Kumar Kolla
, et al.
·
Synthetic Communications
·
6
Synthesis of All Enantiomerically Pure Diastereomers of Aprepitant
2010
·
Srinivas Gangula
, Chandrashekhar R. Elati
, et al.
·
Synthetic Communications
·
4
Towards the Development of a Commercial Process To Produce Muvalaplin. Part I: Preparation of a Key Intermediate by an Evans Auxiliary-Assisted Asymmetric Alkylation
2026
·
Daniel P. Walker
, Matthew J. Genzink
, et al.
·
Organic Process Research & Development
·
2
Substrate Modification Approach to Achieve Efficient Resolution: Didesmethylcitalopram: A Key Intermediate for Escitalopram
2007
·
Chandrashekar R. Elati
, Naveenkumar Kolla
, et al.
·
Organic Process Research & Development
·
2
Development of a Scalable Manufacturing Process for Kv1.3 Antagonist LY3972406 Hemiglutarate Hemihydrate
2026
·
Xiaoyong Li
, Joel R. Calvin
, et al.
·
Organic Process Research & Development
·
1
An Improved Process for Repaglinide via an Efficient and One Pot Process of (1S)-3-methyl-1-(2-piperidin-1-ylphenyl)butan-1-amine – A Useful Intermediate
2006
·
Naveenkumar Kolla
, Chandrashekar R. Elati
, et al.
·
CHIMIA International Journal for Chemistry
·
1
PDF
Polymorphic study of donepezil hydrobromide
2005
·
Chandrashekar R. Elati
, Pravinchandra J. Vankawala
, et al.
·
Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry
·
1
Toward the Development of a Commercial Process to Produce Muvalaplin. Part II: Preparation of the Drug Substance
2026
·
Daniel P. Walker
, John R. Rizzo
, et al.
·
Organic Process Research & Development
A new method for the one-pot synthesis of symmetrical, tertiary benzylic amines via Ir4(CO)12 catalyzed reductive amination of benzaldehydes
2026
·
Daniel P. Walker
, Matthew J. Genzink
, et al.
·
SSRN Electronic Journal
Scalable synthesis of 3-amino-2, 2-dimethylpropanamide: A key intermediate of Aliskiren
2014
·
B. Sudhakar Reddy
, Srinivas Gangula
, et al.
Structural identification, characterization and synthesis of impurities of Naproxcinod
2014
·
Anitha Naredla
, Srinivas Gangula
, et al.
ChemInform Abstract: Improved Process for Paroxetine Hydrochloride Substantially Free from Potential Impurities.
2013
·
Srinivas Gangula
, Naveen Kumar Kolla
, et al.
·
ChemInform
Recycling of undesired isomers of key intermediate for aprepitant
2009
·
Srinivas Gangula
, Chandrashekar R. Elati
, et al.
·
Green Chemistry Letters and Reviews
PDF
ChemInform Abstract: Novel Synthesis of Fosphenytoin: Anticonvulsant Prodrug.
2009
·
Chandrashekar R. Elati
, Srinivas Gangula
, et al.
·
ChemInform
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Works count:
25
Citation count:
211
H-index:
10
I10-index:
11
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