Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Chie Kadowaki"'
Autor:
Chie Kadowaki, Yoshinori Kohmura, Donald R. Gauthier, Kazunobu Igawa, David A. Conlon, Shinji Kato, Shigemitsu Okada, Anthony O. King, Yong-Li Zhong, Brenda Pipik, Akihiro Takezawa, Robert A. Reamer, Jaemoon Lee, Hua Zhou, David Askin
Publikováno v:
Organic Process Research & Development. 12:1245-1252
A practical and efficient synthesis of the potent HIV integrase inhibitor 1 is described. Starting from readily available 3,4-dihydro-2H-pyran, the six-step synthesis features a through process without purification of any of the intermediates until t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a28fdd0a749b0c7caddc656cea00d32a
https://doi.org/10.1021/op800153y
https://doi.org/10.1021/op800153y
Autor:
Benjamin Marcune, Sandor Karady, Ross A. Miller, Stan S. Hall, Toshiaki Mase, Kenneth J. Fitch, Kenji Maeda, Satoshi Kii, J. J. Dannenberg, Chie Kadowaki, David M. Tschaen, Robert A. Reamer, Kenichi Asakawa
Publikováno v:
Tetrahedron Letters. 46:5081-5084
2-Lithio benzimidazoles were acylated with esters, lactones, and lactams. The tetrahedral hemiacetal intermediates responsible for the efficient conversion were characterized by low temperature NMR.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b4fd9c2179ddba938927bffe010da03
https://doi.org/10.1016/j.tetlet.2005.05.068
https://doi.org/10.1016/j.tetlet.2005.05.068
Autor:
Chie Kadowaki, Isao Kadota, Stephan Thorand, Philip Wai Hong Chan, Yoshinori Yamamoto, Kumi Sato, Choul Hong Park, Hiroyoshi Takamura
Publikováno v:
Tetrahedron. 58:1799-1816
Stereocontrolled syntheses of the AB and EFGH ring systems of gambierol ( 1 ) are described. The two key intermediates 3 and 55 , representing the AB and EFGH ring frameworks, were prepared from 2-deoxy- d -ribose via linear sequences. Brown's asymme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d88d9bd5502680f5a1fac60e6845d264
https://doi.org/10.1016/s0040-4020(02)00039-x
https://doi.org/10.1016/s0040-4020(02)00039-x
Publikováno v:
Tetrahedron Letters. 42:6199-6202
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d284570614df75b324c4b232780f477f
https://doi.org/10.1016/s0040-4039(01)01205-9
https://doi.org/10.1016/s0040-4039(01)01205-9
Publikováno v:
Tetrahedron Letters. 41:5769-5772
A new strategy for the convergent assembly of six-membered polycyclic ether ring fragments has been developed based upon the novel reaction between vinylstannanes with triflates in the presence of a strong base. The application of the present method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1d4a696cda345fd127bda0902819fd8
https://doi.org/10.1016/s0040-4039(00)00952-7
https://doi.org/10.1016/s0040-4039(00)00952-7
Publikováno v:
Tetrahedron Letters. 39:6369-6372
Stereoselective synthesis of the H ring of gambierol was achieved from 2-deoxy-D-ribose by using the intramolecular reaction of allylstannane with aldehyde as a key step. Modified Stille coupling was successfully applied for the construction of the t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9b58ae83fe6238ee2fa9257efd408e8
https://doi.org/10.1016/s0040-4039(98)01311-2
https://doi.org/10.1016/s0040-4039(98)01311-2
Publikováno v:
Tetrahedron Letters. 42:6195-6197
The EFGH ring segment of gambierol was synthesized from 2-deoxy- d -ribose in 40 steps. The present synthesis includes a SmI 2 -mediated reductive cyclization and a Pd-catalyzed coupling of enol triflate with a zinc bis-homoenolate as key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56a286b20452527045918174c40970eb
https://doi.org/10.1016/s0040-4039(01)01204-7
https://doi.org/10.1016/s0040-4039(01)01204-7
Autor:
Chie Kadowaki, Shinichi Saito, Yoshinori Yamamoto, Isao Kadota, Vladimir Gevorgyan, Matthew M. Salter
Publikováno v:
ChemInform. 28
Palladium catalyzed addition of certain carbon pronucleophiles 2 to conjugated enynes 1 afforded the corresponding allenes 3 in good to excellent yields. The most reactive methynes such as methylmalononitrile 2c enabled to undergo double addition lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ca68eb341cc32ded55e16eb3818b337
https://doi.org/10.1002/chin.199748087
https://doi.org/10.1002/chin.199748087
Publikováno v:
ChemInform. 29
Stereoselective synthesis of the H ring of gambierol was achieved from 2-deoxy-D-ribose by using the intramolecular reaction of allylstannane with aldehyde as a key step. Modified Stille coupling was successfully applied for the construction of the t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50714e0be6a164cdbf9f11875ae07501
https://doi.org/10.1002/chin.199845268
https://doi.org/10.1002/chin.199845268
Publikováno v:
ChemInform. 33
The EFGH ring segment of gambierol was synthesized from 2-deoxy- d -ribose in 40 steps. The present synthesis includes a SmI 2 -mediated reductive cyclization and a Pd-catalyzed coupling of enol triflate with a zinc bis-homoenolate as key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e072dc9fe0bbbff53cf68c5bb8b876c5
https://doi.org/10.1002/chin.200202256
https://doi.org/10.1002/chin.200202256