Zobrazeno 1 - 10
of 150
pro vyhledávání: '"Gregory B. Dudley"'
Autor:
A. C. Martin, Jessica A. Rogers, Paratchata Batsomboon, Alec E. Morrison, Ron R. Ramsubhag, Brian V. Popp, Gregory B. Dudley
Publikováno v:
ACS Omega, Vol 6, Iss 44, Pp 30108-30114 (2021)
Externí odkaz:
https://doaj.org/article/79549bd8360e4683990be2433cf6bb77
Publikováno v:
Molecules, Vol 20, Iss 12, Pp 21672-21680 (2015)
Temporary superheating and sustained nucleation-limited “superboiling” of unstirred liquids above the normal atmospheric boiling point have been documented during microwave heating. These phenomena are reliably observed under prescribed condition
Externí odkaz:
https://doaj.org/article/71d72c624773460ea022ef1cbc55d60c
Autor:
Sami F. Tlais, Gregory B. Dudley
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 1287-1292 (2012)
The synthesis of four candidate stereoisomers of cephalosporolide H is described, made possible by a zinc-chelation strategy for controlling the stereochemistry of oxygenated 5,5-spiroketals. The same strategy likewise enables the first stereocontrol
Externí odkaz:
https://doaj.org/article/3935109c579440aa9113928377663b09
Autor:
Sami F. Tlais, Gregory B. Dudley
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 570-577 (2011)
A highly efficient synthesis of oxygenated 5,5-spiroketals was performed towards the synthesis of the cephalosporolides. Gold(I) chloride in methanol induced the cycloisomerization of a protected alkyne triol with concomitant deprotection to give a s
Externí odkaz:
https://doaj.org/article/b1addb551023412bb0a19ece118486c0
Publikováno v:
Molecules, Vol 14, Iss 12, Pp 5216-5222 (2009)
The four-step, asymmetric synthesis of a chiral propargyl alcohol 1 from (R)-pantolactone is described. A key feature of the synthesis is a diastereoselective acetylide addition to a chiral α-alkoxy-aldehyde 7, in which unusual Felkin selectivity is
Externí odkaz:
https://doaj.org/article/52f58cf6d0034b06b3d6acfe1dfc9ed5
Autor:
Susana S. Lopez, Gregory B. Dudley
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 4, Iss 1, p 44 (2008)
2-Benzyloxy-1-methylpyridinium triflate (1) is emerging as a mild, convenient, and in some cases uniquely effective new reagent for the synthesis of benzyl ethers and esters. This article provides a revised benzyl transfer protocol in which N-methyla
Externí odkaz:
https://doaj.org/article/8d32df38082a4b1cbf1b928ed3db1d96
Autor:
Matthew R. Blake, Ryan T. Gardner, Haihong Jin, Melanie A. Staffenson, Nicole J. Rueb, Amy M. Barrios, Gregory B. Dudley, Michael S. Cohen, Beth A. Habecker
Publikováno v:
ACS Chem Neurosci
Chondroitin Sulfate Proteoglycans (CSPGs) prevent sympathetic nerve regeneration in the heart after myocardial infarction, and prevent central nerve regrowth after traumatic brain injury and spinal cord injury. Currently there are no small molecule t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3d285627535a2891dfca6d7b2b2c223
https://doi.org/10.1021/acschemneuro.1c00854
https://doi.org/10.1021/acschemneuro.1c00854
Publikováno v:
Physical Chemistry Chemical Physics. 24:2794-2799
Selective microwave heating of polar agglomerates in solution accelerates an aryl Claisen rearrangement.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79b653a4c5661a1e761e84c7c2dddbc9
https://doi.org/10.1039/d1cp04883j
https://doi.org/10.1039/d1cp04883j
Autor:
Tengda Jin, Jingyue Yang, A. C. Martin, Keju Sun, Liyan Zhang, Yingjie Guo, Gregory B. Dudley
Publikováno v:
The Journal of Organic Chemistry. 86:16716-16724
The development of efficient methods for the synthesis of substituted polycyclic arenes with various topologies is in high demand due to their excellent electrical and optical properties. In this work, a series of gem-dimethylcyclopentane-fused arene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::943469e30bbf77a6d3b717ebca021fdf
https://doi.org/10.1021/acs.joc.1c01957
https://doi.org/10.1021/acs.joc.1c01957
Autor:
Amir Tavakoli, Gregory B. Dudley
Publikováno v:
The Journal of organic chemistry. 87(21)
Alkyne [2 + 2 + 2] cyclotrimerization is a strategically attractive but tactically challenging approach to the synthesis of highly substituted benzene rings. Here, a bimolecular regioselective cyclotrimerization is applied to the total synthesis of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebc0e1cdfe32c40ec3f25ec93e351224
https://pubmed.ncbi.nlm.nih.gov/36215202
https://pubmed.ncbi.nlm.nih.gov/36215202