Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Daniel E. Patterson"'
Publikováno v:
Administrative Theory & Praxis. 41:186-188
Reviewed by Daniel E. Patterson and Sharon MastracciUniversity of Utah“You don’t have to choose between being scientific and being compassionate.” (Sapolsky, 2017, p. 675)In Descartes’ Error: Emoti...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a649705ab143746573a1aa241a0235c
https://doi.org/10.1080/10841806.2018.1517519
https://doi.org/10.1080/10841806.2018.1517519
Autor:
B. Liu, Vassil I. Elitzin, J. Powers, Daniel E. Patterson, Roman Davis, Elie Amine Tabet, Chong Pek Yoke, Matthew Salmons, M. Toczko, Mark A. Hatcher, Kae M. Bullock, M. Jackson
Publikováno v:
Topics in Catalysis. 55:446-452
Transition metal catalysis by Cu (CF3Cu), Ir (C–H activation), and Ru (ring-closing metathesis) were applied to prepare a complicated tetra substituted pyrazolopyridine drug candidate at GlaxoSmithKline. CuI/FSO2CF2CO2Me was utilized to install a C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86a49cac259c11c359deec285714ae7c
https://doi.org/10.1007/s11244-012-9809-z
https://doi.org/10.1007/s11244-012-9809-z
Autor:
Alan Millar, Claire Crawford, Sandeep B. Kedia, Bobby N. Glover, Jeremiah D. Powers, Christopher J. Nichols, Malcolm B. Berry, Mark B. Mitchell, Michael S. McClure, Brian C. Crump, Daniel E. Patterson, Darren Caine
Publikováno v:
European Journal of Organic Chemistry. 2012:3561-3565
A highly selective method for the alkoxycarboxylation and acylation of primary alcohols of pyranose derivatives is described. The reaction is high yielding and proceeds under mild conditions with 0.15–1 mol-% Sc(OTf)3 used in combination with anhyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7aefdcbbaf58962295c371c723bf7cc4
https://doi.org/10.1002/ejoc.201200261
https://doi.org/10.1002/ejoc.201200261
Autor:
Michael P LeBlanc, Jeremiah D. Powers, Erwin Irdam, Martin H. Osterhout, Tyler Sharkey, Daniel E. Patterson, Emily Boehler
Publikováno v:
Organic Process Research & Development. 13:900-906
A large-scale synthesis of denagliptin tosylate has been developed. The efficiency of the synthesis has been improved from the initially scaled route by changing the order of steps (performing a dehydration at a late stage). The key step of the synth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e3fa5bfcc4d13115c925fb4d9cfab25
https://doi.org/10.1021/op900178d
https://doi.org/10.1021/op900178d
Autor:
Roman Davis, Andrew D. Brown, Matthew J. Sharp, Bing Liu, Bobby N. Glover, Russ N. Fitzgerald, Lynda A. Jones, Kim A. Harvey, Daniel E. Patterson
Publikováno v:
Organic Process Research & Development. 13:297-302
Three efficient syntheses of sodelglitazar (1) have been developed. In particular, the third synthesis avoids the use of zinc and eliminates the resulting heavy metal waste stream as well as the potential genotoxic methanesulfonate in the two earlier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::733f09fb456afe43dbf8e2efff278e40
https://doi.org/10.1021/op8002294
https://doi.org/10.1021/op8002294
Autor:
Kristjan S. Gudmundsson, Mark D. Trone, Boggs Sharon Davis, Richard T. Matsuoka, Shiping Xie,‡ and, Xiaoming Zhou, Vicente Samano, Daniel E. Patterson, Lynda A. Jones, Alan Millar, Jeremy D. Cobb
Publikováno v:
Organic Process Research & Development. 11:539-545
An efficient asymmetric synthesis of N-[(1R)-6-chloro-2,3,4,9-tetrahydro-1H-carbazol-1-yl]-2-pyridinecarboxamide 1, a potential treatment for human papillomavirus infections, is described. The key step in the synthesis of this molecule is an asymmetr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71441076ee72c0a2ed81b9764640ea79
https://doi.org/10.1021/op060223v
https://doi.org/10.1021/op060223v
Autor:
Martin H. Osterhout, and Christopher G. Henry, Shiping Xie, Thomas D. Roper, Lynda A. Jones, Daniel E. Patterson
Publikováno v:
Organic Process Research & Development. 11:624-627
4-Fluoro-β-(4-fluorophenyl)-l-phenylalanine 1 was synthesized by the asymmetric phase-transfer catalyzed alkylation of tert-butyl glycinate-benzophenone Schiff base using the cinchona alkaloid derived catalyst 6. Upon scaling, it was observed that t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de196eaa578362898d8c4c47c5129caf
https://doi.org/10.1021/op060190j
https://doi.org/10.1021/op060190j
Publikováno v:
Chemistry - A European Journal. 7:3768-3775
Kinetic resolutions and kinetic asymmetric transformations (KAT) as well as dynamic kinetic resolutions and dynamic kinetic asymmetric transformations (DYKAT) are important synthetic protocols. The feasibility of KAT and DYKAT processes for asymmetri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7f2e2e826c4e7fa489c67a2f1a62a1a
https://doi.org/10.1002/1521-3765(20010903)7:17<3768::aid-chem3768>3.0.co
https://doi.org/10.1002/1521-3765(20010903)7:17<3768::aid-chem3768>3.0.co
Autor:
Barry M. Trost, Daniel E. Patterson
Publikováno v:
Chemistry - A European Journal. 5:3279-3284
The four contiguous stereocenters of (−)-swainsonine were efficiently set in a 15-step synthesis with a 15 % overall yield and >99% ee. In order to differeniate the double bond in the key building block oxazolidin-2-one 2, a synthetic equivalent of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef767ea3bdc4f9503846a24f050cc78a
https://doi.org/10.1002/(sici)1521-3765(19991105)5:11<3279::aid-chem3279>3.0.co
https://doi.org/10.1002/(sici)1521-3765(19991105)5:11<3279::aid-chem3279>3.0.co
Autor:
Darren Caine, Sandeep B. Kedia, Mark B. Mitchell, Bobby N. Glover, Christopher J. Nichols, Jeremiah D. Powers, Brian C. Crump, Daniel E. Patterson, Malcolm B. Berry, Michael S. McClure, Alan Millar, Claire Crawford
Publikováno v:
European Journal of Organic Chemistry. 2012
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::329d7a31f941b566eeebd42a096e06c0
https://doi.org/10.1002/ejoc.201290048
https://doi.org/10.1002/ejoc.201290048