Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Asha Budakoti"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 932-963 (2021)
Functionalized tetrahydropyran (THP) rings are important building blocks and ubiquitous scaffolds in many natural products and active pharmaceutical ingredients (API). Among various established methods, the Prins reaction has emerged as a powerful te
Externí odkaz:
https://doaj.org/article/dfb1ac9cc28d40fbafad4db6a5346b7a
Publikováno v:
Molbank, Vol 2009, Iss 3, p M614 (2009)
Reaction of dibenzalacetone with hydrazine hydrate and formic acid yielded a novel 2-pyrazoline 1, characterized by ESI-MS, FT-IR, UV, 1HNMR and 13CNMR data and microanalysis.
Externí odkaz:
https://doaj.org/article/d15b827e809e4a6e8003a74f8db7ce51
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 932-963 (2021)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
Functionalized tetrahydropyran (THP) rings are important building blocks and ubiquitous scaffolds in many natural products and active pharmaceutical ingredients (API). Among various established methods, the Prins reaction has emerged as a powerful te
Publikováno v:
Organic Chemistry Frontiers. 5:2610-2614
α-Arylation of ketones with electron rich arenes via sp2(C)–H has been achieved by the reaction of α-phenylselanylketones using organic photoredox catalysis. The reaction proceeds via an α-methylene ketone radical generated by sp3(C)–SePh acti
Publikováno v:
Tetrahedron Letters. 51:2975-2978
Synthesis of optically pure 2,3,4-trisubstituted tetrahydrofurans is described employing a two-step Michael-Evans aldol cyclization strategy. The approach is successfully applied for the total synthesis of furano lignan natural product (+)-magnolone.
Publikováno v:
European Journal of Medicinal Chemistry. 44:1317-1325
In an effort to develop potent antiamoebic agents, we have synthesized chalcones ( 1 – 8 ), amino-5-substituted-(3-phenyl(2-pyrazolinyl))methane-1-thione derivatives ( 1a – 8a ) and 2-(5-substituted-3-phenyl-2-pyrazolinyl)-1,3-thiazolino[5,4- b ]
Publikováno v:
European Journal of Medicinal Chemistry. 42:544-551
Reaction of neutral NS bidentate ligands, 1-N-substituted thiocarbamoyl-3,5-diphenyl-2-pyrazolines, isolated by cyclization of chalcone with N-4-substituted thiosemicarbazide of aromatic amines (1-8), with [Pd(DMSO)(2)Cl(2)] (DMSO=dimethylsulfoxide)
Publikováno v:
ChemInform. 41
A concise method is developed and the product (IIIb) is used as starting material for the total synthesis of (+)-magnolone (IV).
Publikováno v:
Molbank, Vol 2009, Iss 3, p M614 (2009)
Reaction of dibenzalacetone with hydrazine hydrate and formic acid yielded a novel 2-pyrazoline 1 , characterized by ESI-MS, FT-IR, UV, 1 HNMR and 13 CNMR data and microanalysis. Keywords: dibenzalacetone; hydrazine hydrate; pyrazoline; 5-phenyl-3-[(
Publikováno v:
ChemInform. 39
A variety of 3-(3-bromo phenyl)-5-phenyl-1-(thiazolo [4,5-b] quinoxaline-2-yl)-2-pyrazoline were obtained by the refluxing of 1-N-thiocarbamoyl 3,5-diphenyl-2-pyrazoline with 2,3-dichloroquinoxaline. The chemical structures of the compounds were eluc