Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gary D. Madding"'
Autor:
Susanne Kiau, Gary D. Madding, Robert P. Discordia, Victor W. Rosso, Francis J. Okuniewicz, John J. Venit
Publikováno v:
The Journal of Organic Chemistry. 69:4256-4261
Herein we present a novel route to enantiomerically enriched chiral alpha-substituted carboxylic acids by crystallization-induced dynamic resolution (CIDR) of their diastereomeric salts with chiral amines. Thus, the racemic alpha-bromo acid 3 is conv
Autor:
Gary D. Madding, Bang-Chi Chen, J. Gregory Reid, Tonya P Robinson, Michael J. Humora, William Early, Sandra L. Quinlan, John J. Venit, Edward J. Delaney, Paul A. Jass, William J. Winter
Publikováno v:
Tetrahedron: Asymmetry. 9:1337-1340
BMS-180448, (3S,4R)- 2 , was prepared in 63% yield via a facile method which involved a new regio- and stereoselective ring opening of epoxide (3S,4S)- 12 with the potassium dianion of cyanoguanidine 11 .
Autor:
Jack Z. Gougoutas, John C. Harris, and Donald L. Wedding, David A. Thurston, Gus A. Kodersha, David A. Lust, William Early, Dennis Ronald D, Daniel H. Kim, Atul S. Kotnis, Dominique Thoraval, William J. Winter, James L. Berg, Merrill L. Davies, Peter J. Bernot, James H. Simpson, Jerome L. Moniot, Neal G. Anderson, Paul A. Jass, Douglas W. Phillipson, Kai Tse, Droghini Roberto, Andrew Nguyen, Thomas D. Ary, Lajeunesse Jean, John D. Dimarco, Venkatapuram A. Palaniswamy, Hoang D. Do, Gary D. Madding, Oscar W. Haas, Yeung Y. Chan, Polomski Robert E, Rajan P. Deshpande, Chien-Kuang Chen, John A. Grosso, Sandeep P. Modi
Publikováno v:
Organic Process Research & Development. 1:300-310
5-Fluoro-3-[3-[4-(5-methoxy-4-pyrimidinyl)-1-piperazinyl]propyl]-1H-indole dihydrochloride (1) facilitates 5-HT neurotransmission and was an antidepressant drug candidate. The development of a safe, rugged process for the large-scale, chromatography-
Publikováno v:
ChemInform. 24
Two new and improved syntheses of the antiarrhythmic drug Encainide, 1, are presented. The first approach is based on the condensation of 2-picolyllithium with the p-anisoyl amide of methyl anthranilate, 3, followed by a series of catalytic hydrogena
Autor:
Gary D. Madding
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[58986-28-0] C5H7NaO3 (MW 138.11) InChI = 1S/C5H8O3.Na/c1-2-8-5(7)3-4-6;/h3-4,6H,2H2,1H3;/q;+1/p-1/b4-3-; InChIKey = ITWVTNYFGKFDGE-LNKPDPKZSA-M (a three-carbon β-dicarbonyl building block) Alternate Names: ethyl formylacetate, sodium salt. Solubili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de1cfea9a3dce01b1dc1614b43f21b4f
https://doi.org/10.1002/047084289x.re091
https://doi.org/10.1002/047084289x.re091
Publikováno v:
Journal of Heterocyclic Chemistry. 22:1121-1126
The synthesis and x-ray crystal structure of BMY 13754, a 1,2,4-triazolin-3-one under clinical evaluation as an antidepressant agent, is described. Several synthetic strategies are discussed.
Publikováno v:
The Journal of Organic Chemistry. 32:308-317
Autor:
Gary D. Madding
Publikováno v:
The Journal of Organic Chemistry. 37:1853-1854