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Chemical Communications (Cambridge, England)|November 26, 2011
Strength from weakness: opportunistic CH···O hydrogen bonds differentially dictate the conformational fate in solid and solution statesAmol M Vibhute, Rajesh G Gonnade, R S Swathi, et al.
Chemical Record (New York, N.Y.)|May 24, 2021
Advanced Chemical Methods for Stereoselective Sialylation and Their Applications in Sialoglycan SynthesesAmol M Vibhute, Naoko Komura, Hide-Nori Tanaka, et al.
Organic & Biomolecular Chemistry|December 11, 2012
Synthesis and characterization of pH-sensitive, biotinylated MRI contrast agents and their conjugates with avidinSandip M Vibhute, Jörn Engelmann, Tatjana Verbić, et al.
RSC Advances|January 10, 2017
Synthesis of dimeric analogs of adenophostin A that potently evoke Ca<sup>2+</sup> release through IP<sub>3</sub> receptorsAmol M Vibhute, Poornenth Pushpanandan, Maria Varghese, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 26, 2021
Azide-Functionalized Derivatives of the Virulence-Associated Sugar Pseudaminic Acid: Chiral Pool Synthesis and Labeling of BacteriaAmol M Vibhute, Hideki Tamai, Dana Logviniuk, et al.
The Journal of Organic Chemistry|November 30, 2020
Stereoselective Synthesis of Diglycosyl Diacylglycerols with Glycosyl Donors Bearing a β-Stereodirecting 2,3-Naphthalenedimethyl Protecting GroupNahoko Yagami, Amol M Vibhute, Hide-Nori Tanaka, et al.
Pharmaceutics|April 26, 2025
Translational Pharmacokinetic-Pharmacodynamic Modeling of a Novel Oral Dihydroorotate Dehydrogenase (DHODH) Inhibitor, HOSU-53 (JBZ-001)Joo Young Na, Min Hai, Kyeongmin Kim, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 20, 2020
Quantification of Noncovalent Interactions in Azide-Pnictogen, -Chalcogen, and -Halogen ContactsMarkus Bursch, Lukas Kunze, Amol M Vibhute, et al.
The Journal of Organic Chemistry|December 11, 2025
Pd- and Cu-Cocatalyzed Anaerobic Olefin AminoborationSaurabh S Satpute, Clayton T West, Hannah C Wendlandt, et al.
Biochimica Et Biophysica Acta. General Subjects|March 6, 2022
Structure-based design of UDP-GlcNAc analogs as candidate GnT-V inhibitorsAmol M Vibhute, Hide-Nori Tanaka, Sushil K Mishra, et al.
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