Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Alexander Buitrago Santanilla"'
Publikováno v:
The Power of High-Throughput Experimentation: Case Studies from Drug Discovery, Drug Development, and Catalyst Discovery (Volume 2) ISBN: 9780841297555
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bab655ca0269488fa2fe45e419009b6
https://doi.org/10.1021/bk-2022-1420.ch001
https://doi.org/10.1021/bk-2022-1420.ch001
Autor:
Marion H. Emmert, Matthieu Jouffroy, David C. Leitch, Alexander Buitrago Santanilla, Gemma Cook, Amanda Dombrowski, Nathan Gesmundo, Dipannita Kalyani, Mycah Uehling, Michael Wleklinski, Nicole C. Goodwin, Katherine Honicker, Jonathan Latham, Katherine M. P. Wheelhouse, Sabine Fenner, Matthew P. Whiting, Chunrui Sun, Ji Qi, Feng Peng, Niki R. Patel, Danielle Schultz, Orion Staples, Jacob S. Mohar, Daniel J. Mindiola, Victoria Dimakos, Stephen G. Newman, Stig D. Friis, Erik Weis, Magnus J. Johansson
'High-throughput experimentation (HTE) is an emerging and powerful approach to problems in organic chemistry and homogeneous catalysis. This book is targeted at both experts and those new to the field who are seeking general perspectives and design p
Autor:
Ian W. Davies, Melodie Christensen, Alexander Buitrago Santanilla, Louis-Charles Campeau, Spencer D. Dreher
Publikováno v:
Organic Letters. 17:3370-3373
The non-nucleophilic organic superbase P2Et phosphazene can enable a broad range of palladium-catalyzed cross-coupling reactions, including C-C, C-N, and C-O couplings of aryl chlorides, bromides, and iodides at room temperature. The mildness and sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82c805a2fede938e92a9e12afeabd37b
https://doi.org/10.1021/acs.orglett.5b01648
https://doi.org/10.1021/acs.orglett.5b01648
Autor:
Kevin P. Bateman, Spencer D. Dreher, Yong Liu, Ian W. Davies, Zhi-Cai Shi, Tim Cernak, Christopher J. Welch, Erik L. Regalado, Tony Pereira, Roy Helmy, Jonathan Schneeweis, Louis-Charles Campeau, Simon Berritt, Alexander Buitrago Santanilla, Petr Vachal, Michael Shevlin, Philippe G. Nantermet
Publikováno v:
Science. 347:49-53
Breaking through the milligram floor When chemists synthesize compounds, the threshold for success is at least a milligram of product. This has been true for decades—even though biochemical assays have long since descended into microgram territory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2fc5f0c9b37a015f4ea6f9a68db07fd
https://doi.org/10.1126/science.1259203
https://doi.org/10.1126/science.1259203
Autor:
Melodie Christensen, Louis-Charles Campeau, Spencer D. Dreher, Ian W. Davies, Alexander Buitrago Santanilla
Publikováno v:
ChemInform. 46
The organic superbase P2-Et is shown to possess distinct reactivity across a diverse set of cross-coupling reactions at room temperature.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c70f012d4bea19e4757966dfccf76d2
https://doi.org/10.1002/chin.201545162
https://doi.org/10.1002/chin.201545162
Autor:
Alexander, Buitrago Santanilla, Erik L, Regalado, Tony, Pereira, Michael, Shevlin, Kevin, Bateman, Louis-Charles, Campeau, Jonathan, Schneeweis, Simon, Berritt, Zhi-Cai, Shi, Philippe, Nantermet, Yong, Liu, Roy, Helmy, Christopher J, Welch, Petr, Vachal, Ian W, Davies, Tim, Cernak, Spencer D, Dreher
Publikováno v:
Science (New York, N.Y.). 347(6217)
At the forefront of new synthetic endeavors, such as drug discovery or natural product synthesis, large quantities of material are rarely available and timelines are tight. A miniaturized automation platform enabling high-throughput experimentation f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7a317f19719ddd791422174652ee0100
https://pubmed.ncbi.nlm.nih.gov/25554781
https://pubmed.ncbi.nlm.nih.gov/25554781
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
(S,S)-[447440-43-9] C13H18ClNOSi (MW 267.83) InChI = 1S/C13H18ClNOSi/c1-4-10-17(14)15(3)11(2)13(16-17)12-8-6-5-7-9-12/h4-9,11,13H,1,10H2,2-3H3/t11-,13+,17?/m0/s1 InChIKey = XHCRAANIMMYPDV-APBZJUGRSA-N (R,R)-[596851-24-0] InChI = 1S/C13H18ClNOSi/c1-4-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bee14d880b9663dc3f66ca35647422e
https://doi.org/10.1002/047084289x.rn01444
https://doi.org/10.1002/047084289x.rn01444
Publikováno v:
ChemInform. 41
A new class of N-heteroaryl hydrazones has been developed as an alternative to N-acylhydrazones and 2-aminophenol-derived imines in asymmetric allylation, crotylation, and cinnamylation reactions with chiral allylchlorosilanes. The hydrazones are rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aed60da8ba6f0833833f4af3c1f9ff58
https://doi.org/10.1002/chin.201027058
https://doi.org/10.1002/chin.201027058
Publikováno v:
Organic letters. 12(4)
A new class of N-heteroaryl hydrazones has been developed as an alternative to N-acylhydrazones and 2-aminophenol-derived imines in asymmetric allylation, crotylation, and cinnamylation reactions with chiral allylchlorosilanes. The hydrazones are rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a9008110019a2759ab75de6c64498cb
https://pubmed.ncbi.nlm.nih.gov/20085348
https://pubmed.ncbi.nlm.nih.gov/20085348
Publikováno v:
Synfacts. 2010:0427-0427
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08eb546147ecc315341761b266e36c4b
https://doi.org/10.1055/s-0029-1219482
https://doi.org/10.1055/s-0029-1219482