Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kurt Vagle"'
Autor:
Kurt Vagle, Michael Leuck, Ken Hill, Jeffrey D. Carter, Jon Taunton-Rigby, Danny P. C. McGee, Dominic J. Anziano, David P. Sebesta, Wolfgang Pieken, Gregory M. Husar, Eric Kropp
Publikováno v:
The Journal of Organic Chemistry. 66:5352-5358
In an effort to offer complementary technology for covalent biomolecule modification (bioconjugation), we have developed a method that exploits the aqueous acceleration of Diels--Alder reactions for this purpose. Three different diene phosphoramidite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6d246810c2e923405baf23895dc34ac
https://doi.org/10.1021/jo0100190
https://doi.org/10.1021/jo0100190
Autor:
and David P. Sebesta, Randall S. Smith, Wolfgang Pieken, Gretchen M. Pratt, Kurt Vagle, Christopher J. Tompkins, T. Brian Hurley, John Yegge, Jeffery C. Mihaichuk
Publikováno v:
Organic Process Research & Development. 4:214-224
Presented is a conceptually novel approach to oligonucleotide synthesis referred to herein as dimethoxytrityl resin product anchored sequential synthesis (DMT PASS). The DMT PASS process is characterized by the reaction of a 3‘-protected nucleoside
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd0ea47848fe164e390107a9d4127d18
https://doi.org/10.1021/op990095t
https://doi.org/10.1021/op990095t
Autor:
Richard M. Pagni, Kurt Vagle, James F. Green, John Siler, Ronald Palmer, George W. Kabalka, Lay Choo Tan, Michael McGinnis
Publikováno v:
The Journal of Organic Chemistry. 61:3496-3500
A series of boronated aluminas was prepared by the reaction of BX3 (X = F, Cl, Br) with alumina or by a two-step synthesis involving the reaction of BH3·Me2S with alumina and then with I2. The modi...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc3c9335653499cf5c633e5a576118e0
https://doi.org/10.1021/jo951077m
https://doi.org/10.1021/jo951077m
Publikováno v:
ChemInform. 35
A novel phosphoramidite reagent was developed to convert terminal hydroxyl groups of oligonucleotides into phosphate monoesters. The reagent’s appearance as a solid foam is advantageous for its manipulation and handling in solid-phase synthesis and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::494ba4dcec5c04a0ac078a0642eebb06
https://doi.org/10.1002/chin.200416175
https://doi.org/10.1002/chin.200416175
Autor:
Kurt Vagle, David P. Sebesta
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[1122-28-7] C5H2N4 (MW 118.10) InChI = 1S/C5H2N4/c6-1-4-5(2-7)9-3-8-4/h3H,(H,8,9) InChIKey = XGDRLCRGKUCBQL-UHFFFAOYSA-N (reagent used for activation of phosphoramidites; oligonucleotide synthesis; nucleophilic catalyst) Physical Data: mp 168–175
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c509c54c479f8a81b9155e354411030
https://doi.org/10.1002/047084289x.rn00166
https://doi.org/10.1002/047084289x.rn00166
Autor:
Charles L. Anderson, Michael McGinnis, Kurt Vagle, Rachel Sick, Nancy Engle, George W. Kabalka, Anna G. Edwards, Richard M. Pagni
Publikováno v:
Scopus-Elsevier
(E)-2-Butenal reacts with B-bromocatecholborane in CD2Cl2 at −78°C to form two species in a 1:1 ratio which does not vary between −20°C and −100°C; IR and NMR experiments (1H–1H COSY and 1H–13C HET...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81ebfeb4fcb08ca7304c361b29cb3e50
http://www.scopus.com/inward/record.url?eid=2-s2.0-1342332633&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-1342332633&partnerID=MN8TOARS