Zobrazeno 1 - 4
of 4
pro vyhledávání: '"W. F. Kiesman"'
Publikováno v:
Flow Chemistry in Organic Synthesis ISBN: 9783132423312
Flow Chemistry in Organic Synthesis
Flow Chemistry in Organic Synthesis
When considering whether to develop a flow-chemistry approach to a particular synthetic route, the criteria of safety, quality, cost, sustainability, scalability, and speed are all considered. This chapter presents a case study of a single reaction,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56737e68da1b4984f51109c5a3bb2098
https://doi.org/10.1055/sos-sd-228-00262
https://doi.org/10.1055/sos-sd-228-00262
Autor:
S. Itsuno, M. S. Kerr, J. Imbrogno, A. Schepartz, Torsten Stelzer, H. Kim, Liam P. Kelly, Klavs F. Jensen, R. Telmesani, S. Moon, A. C. Wicker, M. O’Mahony, S. Ferguson, Thomas Wirth, Matthew O'Brien, Allan S. Myerson, S. A. May, Steven V. Ley, T. H. Tran, Angela Steinauer, T. A. McTeague, Bradley L. Pentelute, Alexander J. Mijalis, H. Seo, A. B. Beeler, C. Bottecchia, K. Gilmore, Evan D. Styduhar, Jun-ichi Yoshida, D.-I. A. Kwok, Anastasios Polyzos, W. F. Kiesman, P. H. Seeberger, G. Koch, Dale A. Thomas, A. C. Sun, S. M. Opalka, Corey R. J. Stephenson, A. G. O’Brien, Rachel L. Beingessner, Y. Mo, T. Noël, Timothy F. Jamison, Ashley R. Longstreet, M. S. Ullah, A. E. Strom, Robert W. Hicklin, Ana A. Folgueiras-Amador, Connor W. Coley, Duncan L. Browne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a2dff96f57b28b9885fcf47f47cf573
https://doi.org/10.1055/b-006-161272
https://doi.org/10.1055/b-006-161272
Publikováno v:
Tetrahedron Letters. 38:1309-1312
β-Bromoenamide esters are coupled stereospecifically to vinylboronic acids via a palladium-catalyzed Suzuki reaction. This cross-coupling proceeds under mild conditions with Pd(OAc) 2 in 95% EtOH at 50 °C and produces amino acids with 1,3-diene sid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a005b910e6defc369e34a74dd7a6534
https://doi.org/10.1016/s0040-4039(97)00065-8
https://doi.org/10.1016/s0040-4039(97)00065-8
Publikováno v:
ChemInform. 28
β-Bromoenamide esters are coupled stereospecifically to vinylboronic acids via a palladium-catalyzed Suzuki reaction. This cross-coupling proceeds under mild conditions with Pd(OAc) 2 in 95% EtOH at 50 °C and produces amino acids with 1,3-diene sid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bb74e398b47786e058855095c0b550e
https://doi.org/10.1002/chin.199724078
https://doi.org/10.1002/chin.199724078