Title : Transition metal catalysed c h bond alkynylation

Type of Material: Thesis
Title: Transition metal catalysed c h bond alkynylation
Researcher: Landge, Vinod
Guide: Balaraman, Ekambaram
Department: Chemical Sciences (CSIR-NCL)
Year: 2019
Language: English
Subject: Life Sciences
Transition metal catalysed
Chemistry
Physical and Basic Sciences
Dissertation/Thesis Note: PhD; 2019
Fulltext: Shodhganga

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035__|a(IN-AhILN)th_459921
040__|dIN-AhILN|aAcSIR)
041__|aeng
100__|eResearcher|aLandge, Vinod
110__|aChemical Sciences (CSIR-NCL)|ein|b
245__|aTransition metal catalysed c h bond alkynylation
260__|c2019|b
502__|bPhD|d2019
518__|d2019|oDate of Award
518__|d2015|oDate of Registration
518__|oDate of Completion|d2019
520__|aGeneral remarks and#61656; All catalysts were purchased from commercial sources and used as received. and#61656; All reactions were carried out under innert atmosphere following standard procedures using schlenk techniques. and#61656; Deuterated solvents for NMR spectroscopic analyses were used as received. All 1H NMR and 13C NMR analysis were obtained using a Bruker or JEOL 200 MHz, 400 MHz or 500 MHz spectrometers. Coupling constants were measured in Hertz. All chemical shifts are quoted in ppm, relative to TMS, using the residual solvent peak as a reference standard. The following abbreviations are used to explain the multiplicities: s = singlet, d = doublet, t = triplet, q = quartet, m = multiplet, br =broad. and#61656; HRMS spectra were recorded at UHPLC-MS (Q-exactive-Orbitrap Mass Spectrometer) using electron spray ionization [(ESI+, +/and#8722; 5kV), solvent medium: water, acetonitrile, methanol and ammonium acetate] technique and mass values are expres
650__|aChemistry|2UGC
650__|aPhysical and Basic Sciences|2AIU
653__|aLife Sciences
653__|aTransition metal catalysed
700__|aBalaraman, Ekambaram|eGuide
856__|uhttp://shodhganga.inflibnet.ac.in/handle/10603/372115|yShodhganga
905__|afromsg

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