Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Louis Matty"'
Autor:
John Y. L. Chung, Louis Matty, George Zhou, Fuh-Rong Tsay, Michael H. Kress, Raymond Cvetovich, M. David Weingarten, Joseph S. Amato, Zhen Li
Publikováno v:
The Journal of Organic Chemistry. 70:8560-8563
A practical synthesis of benzisoxazole 1 and its conversion to α-aryloxyisobutyric acid 2 using 1,1,1-trichloro-2-methyl-2-propanol (chloretone) was developed. Benzisoxazole 1 was formed in high yields by the action of either methanesulfonyl chlorid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1a505976b09bb9fdf22644c4ee1c993
https://doi.org/10.1021/jo051027+
https://doi.org/10.1021/jo051027+
Autor:
Karen M. Conrad, Edward G. Corley, D. L. Hughes, Jacqueline H. Smitrovich, Jerry A. Murry, Genevieve N. Boice, Cecile G. Savarin, Louis Matty
Publikováno v:
Tetrahedron. 60:11367-11374
In this manuscript, an efficient synthesis of a functionalized 4-arylpiperidine is disclosed. Several synthetic approaches towards formation of the key aryl-piperidine sp3 carbon–carbon bond are discussed, including a scalable route to the piperidi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::830d1653f8f194f3a602a9e36bfe661a
https://doi.org/10.1016/j.tet.2004.09.092
https://doi.org/10.1016/j.tet.2004.09.092
Autor:
Louis Matty, Kozo Gbewonyo, Wenjie Li, Hu Essa H, Paul J. Reider, Michel Chartrain, Daniel R. Sidler, Russell Boyd, Edward G. Corley, Jeffrey S. Campbell, Nori Ikemoto, Robert D. Larsen, Richard G. Ball, Nancy Barta
Publikováno v:
Canadian Journal of Chemistry. 80:646-652
The convergent synthesis of a potent α1A-selective adrenoceptor antagonist is described. Salient features of the synthesis include the enzymatic resolution of a racemic dihydropyrimidinone and the use of a palladium coupling reaction in the synthesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::036b92db4e774125c2e875505052b452
https://doi.org/10.1139/v02-079
https://doi.org/10.1139/v02-079
Autor:
Ian W. Davies, Paul J. Reider, Louis Matty, Mark Taylor, Jimmy Ming-Tai Wu, David Hughes, Jean-François Marcoux
Publikováno v:
Tetrahedron Letters. 41:8021-8025
Hydrogen bromide has been demonstrated to provide optimal cis -selectivity in the reduction of 4-chromanone α-hydroxyoxime (25:1 cis / trans ) in 94% yield. This reaction is pivotal in the synthesis of cis -aminochromanol.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11cd95c33fe94fa9d0c6d76d71635567
https://doi.org/10.1016/s0040-4039(00)01404-0
https://doi.org/10.1016/s0040-4039(00)01404-0
Autor:
Raymond J, Cvetovich, John Y L, Chung, Michael H, Kress, Joseph S, Amato, Louis, Matty, M David, Weingarten, Fuh-Rong, Tsay, Zhen, Li, George, Zhou
Publikováno v:
The Journal of organic chemistry. 70(21)
A practical synthesis of benzisoxazole 1 and its conversion to alpha-aryloxyisobutyric acid 2 using 1,1,1-trichloro-2-methyl-2-propanol (chloretone) was developed. Benzisoxazole 1 was formed in high yields by the action of either methanesulfonyl chlo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bc5b108ebe1e096a346655c29fe1abaf
https://pubmed.ncbi.nlm.nih.gov/16209608
https://pubmed.ncbi.nlm.nih.gov/16209608
Autor:
Jacqueline H. Smitrovich, Mark A. Huffman, Joseph F. Payack, Louis Matty, Jonathan D. Rosen, James M. McNamara, Todd D. Nelson, Bridgette Craig
Publikováno v:
ChemInform. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5bef914e03678b3f12dd7a49a57a45b
https://doi.org/10.1002/chin.200517138
https://doi.org/10.1002/chin.200517138
Publikováno v:
The Journal of organic chemistry. 70(1)
An efficient synthesis of the potent KDR inhibitor 3-[5-[[4-(methylsulfonyl)-1-piperazinyl]methyl]-1H-indole-2-yl]quinolin-2(1H)-one (1) is described. The process features a noncryogenic indole boronation and a dicyclohexylamine-mediated Suzuki coupl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e4d0313c69b69ad7a393924ab2d3cca
https://pubmed.ncbi.nlm.nih.gov/15624920
https://pubmed.ncbi.nlm.nih.gov/15624920
Autor:
Mark A. Huffman, Todd D. Nelson, Jacqueline H. Smitrovich, James M. McNamara, Bridgette Craig, Joseph F. Payack, Louis Matty, Jonathan D. Rosen
Publikováno v:
Organic letters. 7(1)
The concise synthesis of a stereochemically rich hNK-1 receptor antagonist is described. The synthesis is highlighted by an S(N)2 reaction of an enantiomerically pure alpha-alkoxy sulfonate (orthogonally protected butane triol), which was prepared by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4462c9978e0459ddd09411474381da7d
https://pubmed.ncbi.nlm.nih.gov/15624976
https://pubmed.ncbi.nlm.nih.gov/15624976
Publikováno v:
Journal of the American Chemical Society. 123(41)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f6ce1c0e6cdf8a8d8631fa5a884541a
https://pubmed.ncbi.nlm.nih.gov/11592910
https://pubmed.ncbi.nlm.nih.gov/11592910
Autor:
Lawrence B. Ebert, Louis Matty
Publikováno v:
Synthetic Metals. 4:345-361
Although both the true intercalation compound “C 13 CrO 3 ” and the commercially available Seloxcette graphite/chromium trioxide mixture are reduced by various inorganic reagents, only the Seloxcette is efficacious in oxidizing primary alcohols t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::415a5b5ea6bb82e79b21d9afc3d2bac2
https://doi.org/10.1016/0379-6779(82)90005-4
https://doi.org/10.1016/0379-6779(82)90005-4