Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Guddeangadi N. Gururaja"'
Autor:
Ankush Gupta, Jaydeepbhai P Jadav, Guddeangadi N Gururaja, Jigarkumar K Vankar, Shankara H Nanjegowda
Publikováno v:
Organic & Biomolecular Chemistry. 19:2473-2480
The direct integration of sulphur and amine groups with 1,1-dibromoalkenes for thioamide synthesis has been achieved in an aqueous medium. The presented green protocol emphasizes the suitability of aqueous media for the thioamidation reaction and ena
Publikováno v:
Molecules, Vol 18, Iss 4, Pp 4357-4372 (2013)
We have recently introduced a new class of chiral ammonium salt catalysts derived from easily available TADDOLs. To get a full picture of the scope of application and limitations of our catalysts we tested them in a variety of different important tra
Externí odkaz:
https://doaj.org/article/b7458e20c7c54265926db07d2d0c9459
Publikováno v:
The Journal of organic chemistry. 87(5)
A mild, greener approach toward thioamide synthesis has been developed. Its unique features include water-mediated reaction with no input energy, additives, or catalysts as well. The presented protocol is attractive with readily available starting ma
Publikováno v:
Organicbiomolecular chemistry. 18(29)
The Mg-mediated conjugate addition of bromoform to a variety of electron-deficient alkenes has been investigated. In the case of nitrodienes and dibenzylideneacetones, tribromomethylated products were isolated, whereas spiro-cyclopropanated products
Publikováno v:
Journal of Thermal Analysis and Calorimetry. 120:1071-1075
We argue that l-alanine thiourea (LATU) 1 (J Therm Anal Calorim 112:1059–1066, 2013) l-valine nickel chloride (LVNiC) 2 (J Therm Anal Calorim 108:887–894, 2012) and l-valine thiourea (LVTU) 3 (J Therm Anal Calorim 119:907–913, 2015) reported by
Publikováno v:
European Journal of Organic Chemistry. 2011:2048-2052
The Mg-mediated conjugate addition of bromoform to enones followed by alcoholysis of the resulting keto tribromides proceeds through an unusual course, affording cyclic orthoester (dihydrofuran) intermediates under neutral workup conditions. However,
Publikováno v:
The Journal of Organic Chemistry. 74:2601-2604
Addition of bromoform to conjugated nitroalkenes in the presence of Mg provided beta-tribromomethyl nitroalkanes in good to excellent yields and diastereoselectivity. These novel Michael adducts, formed under radical conditions, underwent elimination
Autor:
Guddeangadi N. Gururaja, Mario Waser
The field of complex (natural) product syntheses has been dominated by (transition-)metal-catalyzed asymmetric reactions for decades. However, besides the very broad range of different transformations that can be achieved by metal catalysis, the use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29eef08bf6b0bf3d67c6bc903a36d069
https://doi.org/10.1016/b978-0-444-63430-6.00014-x
https://doi.org/10.1016/b978-0-444-63430-6.00014-x
Publikováno v:
ChemInform. 44
Tartaric acid is one of the most prominent naturally occurring chiral compounds. Whereas its application in the production of chiral ligands for metal-catalysed reactions has been exhaustively investigated, its potential to provide new organocatalyst
Autor:
Bichismitha Sahu, Irishi N. N. Namboothiri, Shaikh M. Mobin, Tarun Kumar, Bishwajit Ganguly, Anamitra Chatterjee, Guddeangadi N. Gururaja
Publikováno v:
IndraStra Global.
A novel cage-annulated (bis-homocubyl) vinylidenecarbene has been generated and successfully trapped without any intermediacy of its cycloalkyne isomer. The greater kinetic and thermodynamic stability of the vinylidenecarbene vis-a-vis its cycloalkyn