Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Jerome L. Moniot"'
Autor:
Joseph Wurdinger, Theodor Denzel, Janak Singh, Chris G. Papaioannou, Richard H. Mueller, Rita Fox, Rolf Herter, Peter Schierling, Thomas P. Kissick, Jerome L. Moniot, Christopher M. Cimarusti
Publikováno v:
Organic Process Research & Development. 6:863-868
An efficient synthesis of the monobactam aztreonam [[2S-[2α,3β(Z)]]-3[[(2-amino-4-thiazolyl)[(1-carboxy-1-methylethoxy)imino]acetyl]amino]-2-methyl-4-oxo-1-azetidinesulfonic acid] (1) by acylation of α-aminoazetidinone 22 with the regioselectively
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-
Autor:
Barbara M. Ciaramella, David A. Lust, and Robert E. Polomski, Alan F Feldman, Neal G. Anderson, Steven S. Y. Wang, Linda Moran, Jerome L. Moniot
Publikováno v:
Organic Process Research & Development. 1:211-216
A safe, rugged process for the manufacture of a Monopril intermediate using a trimethylsilyl-mediated Arbuzov reaction was developed. The problems encountered and overcome in iterations from pilot plant to manufacturing are described. The final proce
Publikováno v:
The Journal of Organic Chemistry. 51:3140-3143
La (S)-hydroxymethyl-5 pyrrolidone-2 (preparee a partir de l'acide L-glutamique est condensee avec le benzaldehyde en perhydro phenyl-3 pyrrolo [1,2-c] oxazolone-5; apres alkylation par le bromo-3 cyclohexene puis reduction, on obtient le trans-cyclo
Preparation of phosphinic acids: Michael additions of phosphonous acids/esters to conjugated systems
Publikováno v:
Tetrahedron Letters. 25:4741-4744
A very mild and facile method for the preparation of phosphinic acids via Michael addition of phosphonous acids as well as esters, through an intermediate silyl alkyl phosphonite, to activated conjugated systems is described.
Publikováno v:
Tetrahedron Letters. 19:4617-4620
Autor:
Mary F. Malley, Jack Z. Gougoutas, Thomas P. Kissick, O. Kocy, Jerome L. Moniot, Fox Rita T, Janak Singh, Michael Wong
Publikováno v:
The Journal of Organic Chemistry. 53:205-208
Publikováno v:
Tetrahedron Letters. 25:4737-4740
A very mild and simple method for the preparation of phosphinic acids from phosphonous acids through the intermediacy of silylalkyl phosphonites is described.
Publikováno v:
The Journal of Organic Chemistry. 44:4343-4346