Majid I. Tamboli
National Chemical Laboratory
12 Papers
33 Citations
Majid I. Tamboli is an academic researcher from National Chemical Laboratory. The author has contributed to research in topics: Crystal structure & Nucleophile. The author has an hindex of 5, co-authored 12 publications. Previous affiliations of Majid I. Tamboli include Hoshi University.
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Papers
Identification of Molecular Crystals Capable of Undergoing an Acyl-Transfer Reaction Based on Intermolecular Interactions in the Crystal Lattice
TL;DR: The successful identification of reactive crystals opens up a new method for the detection of molecular crystals capable of exhibiting acyl-transfer reactivity.
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Crystal-to-Crystal Thermal Phase Transformation of Polymorphs of Isomeric 2,3-Naphthalene Diol Ditoluates: Mechanism and Implications for Molecular Crystal Formation and Melting
TL;DR: Isomeric para- and meta-ditoluate derivatives of naphthalene 2,3-diol exhibited polymorphism producing three (Forms 1I, 1II, 1III) and two (forms 2I, 2II) polymorphs each, depending on the solvent and conditions of crystallization as mentioned in this paper.
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Correlation of the solid-state reactivities of racemic 2,4(6)-di-O-benzoyl-myo-inositol 1,3,5-orthoformate and its 4,4'-bipyridine cocrystal with their crystal structures.
TL;DR: The presence of 4,4'-bipyridine molecules in its cocrystal, C21H18O8·C10H8N2, (1)·BP, inhibits the intermolecular benzoyl-group transfer reaction and restricts the solid-state reactivity.
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Clues from Crystal Structures Pave the Way to Access Chiral myo-Inositol Derived Versatile Synthons: Resolution of Racemic 4-O-Allyl-myo-Inositol-1,3,5-Orthoesters via Corresponding Dicamphanates by Crystallization
TL;DR: In this article, the diastereomeric myo-inositol dicamphanates were resolved by crystallization from alcoholic solvents, and the configuration of all these diastereromers was established by conversion to known chiral inositol derivatives as well as by single crystal structure analysis.
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Crystal Structural Analysis of DL-Mandelate Salt of Carvedilol and Its Correlation with Physicochemical Properties
Nanami Hata,Takayuki Furuishi,Majid I. Tamboli,Momiji Ishizaki,Daiki Umeda,Kaori Fukuzawa,Etsuo Yonemochi +6 more
- 20 Jan 2020
TL;DR: A 1:1 salt of carvedilol (CVD), an anti-hypertensive drug, with DL-mandelic acid (DL-MA) was crystallized from ethanol and the structure was characterized by X-ray single-crystal diffraction, revealing salt formation by transfer of an acidic proton from the COOH group of MA to the aliphatic secondary amino NH group of CVD.
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