Follow
Dr. Biswajit Saha, FRSC, London, UK
Dr. Biswajit Saha, FRSC, London, UK
Verified email at amity.edu
Title
Cited by
Cited by
Year
Water as an efficient medium for the synthesis of tetrahydro-β-carbolines via Pictet–Spengler reactions
B Saha, S Sharma, D Sawant, B Kundu
Tetrahedron letters 48 (8), 1379-1383, 2007
832007
Application of modified Pictet–Spengler reaction for the synthesis of thiazolo-and pyrazolo-quinolines
S Duggineni, D Sawant, B Saha, B Kundu
Tetrahedron 62 (14), 3228-3241, 2006
772006
Synthesis of novel N-rich polycyclic skeletons based on azoles and pyridines
S Sharma, B Saha, D Sawant, B Kundu
Journal of Combinatorial Chemistry 9 (5), 783-792, 2007
632007
An insight in anti-malarial potential of indole scaffold: A review
M Chauhan, A Saxena, B Saha
European journal of medicinal chemistry 218, 113400, 2021
502021
Application of the Pictet–Spengler reaction to aryl amine substrates linked to deactivated aromatic heterosystems
B Saha, S Sharma, D Sawant, B Kundu
Tetrahedron 64 (37), 8676-8684, 2008
502008
Generation of highly strained 2, 3-bridged 2H-azirines via cycloaddition reactions of 2-azidobuta-1, 3-dienes and photolysis of the resulting cyclic vinyl azides
K Banert, A Ihle, A Kuhtz, E Penk, B Saha, EU Würthwein
Tetrahedron 69 (11), 2501-2508, 2013
352013
Cu-FeCl3-mediated one-pot multicomponent reaction leading to N-aryl-and N-alkyltriazoles in water
B Saha, S Sharma, D Sawant, B Kundu
Synlett 2007 (10), 1591-1594, 2007
352007
Synthesis of fused polycyclic nitrogen-containing heterocycles via cascade cyclization
B Saha, R Kumar, PR Maulik, B Kundu
Tetrahedron letters 47 (16), 2765-2769, 2006
342006
A p-toluenesulfinic acid-catalyzed three-component Ugi-type reaction and its application for the synthesis of α-amino amides and amidines
B Saha, B Frett, Y Wang, H Li
Tetrahedron Letters 54 (19), 2340-2343, 2013
332013
An expeditious approach to access 2-arylimidazo [1, 2-a] pyridin-3-ol from 2-amino pyridine through a novel Petasis based cascade reaction
Y Wang, B Saha, F Li, B Frett, H Li
Tetrahedron Letters 55 (7), 1281-1284, 2014
232014
Highly Strained 2,3‐Bridged 2H‐Azirines at the Borderline of Closed‐Shell Molecules
K Banert, B Meier, E Penk, B Saha, EU Würthwein, S Grimme, T Rüffer, ...
Chemistry–A European Journal 17 (4), 1128-1136, 2011
232011
Canvassing the aetiology, prognosis and molecular signatures of obstructive sleep apnoea
S Khurana, S Sharda, B Saha, S Kumar, R Guleria, S Bose
Biomarkers 24 (1), 1-16, 2019
142019
An atom-economical and regioselective metal-free C-5 chalcogenation of 8-aminoquinolines under mild conditions
V Kumar, K Banert, D Ray, B Saha
Organic & Biomolecular Chemistry 17 (48), 10245-10250, 2019
132019
An efficient one-pot multicomponent synthesis of tetracyclic quinazolino [4, 3-b] quinazolines by sequential C–N bond formation and copper-mediated aerobic oxidative cyclization
GR Potuganti, DR Indukuri, M Alla
Synlett 29 (13), 1717-1722, 2018
122018
Anti-microbial, anti-oxidant, and anti-breast cancer properties unraveled in yeast carotenoids produced via cost-effective fermentation technique utilizing waste …
S Sinha, S Das, B Saha, D Paul, B Basu
Frontiers in Microbiology 13, 1088477, 2023
102023
Design and identification of novel annomontine analogues against SARS-CoV-2: An in-silico approach
K Waidha, A Saxena, P Kumar, S Sharma, D Ray, B Saha
Heliyon 7 (4), 2021
102021
Observations on the phloem in three species ofMimosa
BC Kundu, B Saha
Experientia 24 (3), 287-288, 1968
101968
Arene ruthenium catalyst MCAT-53 for the synthesis of heterobiaryl compounds in water through aromatic C–H bond activation
A Mehta, B Saha, AA Koohang, MS Chorghade
Organic Process Research & Development 22 (9), 1119-1130, 2018
92018
Phase III trial of molnupiravir in adults with mild SARS-CoV-2 infection in India
N Kumarasamy, B Saha, A Jindal, VB Singh, NC Reddy Podduturi, ...
Topics in Antiviral Medicine, 39-39, 2022
82022
Current development of β-carboline derived potential antimalarial scaffolds
P Kushwaha, V Kumar, B Saha
European Journal of Medicinal Chemistry 252, 115247, 2023
72023
The system can't perform the operation now. Try again later.
Articles 1–20