Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Julie A. Straub"'
Autor:
Valeria R Mas, Kellie J Archer, Catherine I Dumur, Mariano J Scian, Jihee L Suh, Anne L King, Megan E Wardius, Julie A Straub, Marc P Posner, Kenneth Brayman, Daniel G Maluf
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e35526 (2012)
The use of expanded criteria donor kidneys (ECD) had been associated with worse outcomes. Whole gene expression of pre-implantation allograft biopsies from deceased donor kidneys (DDKs) was evaluated to compare the effect of pulsatile pump preservati
Externí odkaz:
https://doaj.org/article/ac6176a498d1445c94656bd17d2b728f
Autor:
Kenneth L. Brayman, Daniel G. Maluf, Catherine I. Dumur, Anne L. King, Kellie J. Archer, Julie A. Straub, Mariano J. Scian, Marc P. Posner, Valeria R. Mas, Megan E. Wardius, Jihee L. Suh
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e35526 (2012)
PLoS ONE
PLoS ONE
Background The use of expanded criteria donor kidneys (ECD) had been associated with worse outcomes. Whole gene expression of pre-implantation allograft biopsies from deceased donor kidneys (DDKs) was evaluated to compare the effect of pulsatile pump
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e2084793a96a4e27e65c7ab8f006054
http://europepmc.org/articles/PMC3335841?pdf=render
http://europepmc.org/articles/PMC3335841?pdf=render
Publikováno v:
ChemInform. 22
Asymmetric allylborations of epoxy aldehydes using tartrate allylboronates (R,R)- and (S,S)- and applications of this chemistry to the highly diastereoselective synthesis of the four hept-1-ene-4,5,6,7-tetrol stereoisomers. The conversion of the arab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f652e76ef877bc4d0f415431e3c9624
https://doi.org/10.1002/chin.199128093
https://doi.org/10.1002/chin.199128093
Publikováno v:
The Journal of Organic Chemistry. 56:3849-3855
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1abf3ee502bea343dc7a5db6a467a4ba
https://doi.org/10.1021/jo00012a015
https://doi.org/10.1021/jo00012a015
Publikováno v:
The Journal of Organic Chemistry. 56:1636-1648
Asymmetric allylborations of epoxy aldehydes using tartrate allylboronates (R,R)- and (S,S)- and applications of this chemistry to the highly diastereoselective synthesis of the four hept-1-ene-4,5,6,7-tetrol stereoisomers. The conversion of the arab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6084fd8227e1770281def02a1b479cc
https://doi.org/10.1021/jo00004a053
https://doi.org/10.1021/jo00004a053
Publikováno v:
The Journal of Organic Chemistry. 56:1649-1655
A highly stereoselective synthesis of the AB disaccharide (4c) of olivomycin A is described. The synthesis features the double asymmetric allylboration of α,β-dialkoxy aldehyde using tartrate allylboronate (S,S)-, which provides triol derivative wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22865b062c5b62d2be61a6f743a5bf90
https://doi.org/10.1021/jo00004a054
https://doi.org/10.1021/jo00004a054
Publikováno v:
The Journal of Organic Chemistry. 55:4117-4126
Les substituants α- et β-alkoxy aldehydes de conformation non restreinte ont un effet negatif sur la stereoselectivite des allylborations asymetriques, contrairement aux formes chirales contenant un groupement alkoxy a conformation restreinte. Pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef61eea8727c13136441f8ea202e435e
https://doi.org/10.1021/jo00300a032
https://doi.org/10.1021/jo00300a032
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c5a12eb1774d3b74ee79334d61a0ec1
https://doi.org/10.1002/chin.199045064
https://doi.org/10.1002/chin.199045064
Autor:
Julie A. Straub, Donald E. Chickering, Jonathan C. Lovely, Huimin Zhang, Bhavdeep Shah, William R. Waud, Howard Bernstein
Publikováno v:
Pharmaceutical Research; Mar2005, Vol. 22 Issue 3, p347-355, 9p
Autor:
William R. Roush, Julie A. Straub
Publikováno v:
Tetrahedron Letters. 27:3349-3352
An efficient (10 step, 17% overall yield), highly diasteroselective total synthesis of disaccharide 3 , corresponding to the AB disaccharide unit of olivomycin A, is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77e23055260f2283c25f5d298a5fc601
https://doi.org/10.1016/s0040-4039(00)84793-0
https://doi.org/10.1016/s0040-4039(00)84793-0