Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes
摘要:
Herein, we describe a convenient method for the synthesis of symmetrical 1,3-dienes employing an oxidative palladium-catalyzed homocoupling of potassium alkenyltrifluoroborates providing products in good yields relative to existing methodologies. This is the first report of a cross-dimerization of potassium alkenyltrifluoroborates. (C) 2009 Elsevier Ltd. All rights reserved.
Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes
摘要:
Herein, we describe a convenient method for the synthesis of symmetrical 1,3-dienes employing an oxidative palladium-catalyzed homocoupling of potassium alkenyltrifluoroborates providing products in good yields relative to existing methodologies. This is the first report of a cross-dimerization of potassium alkenyltrifluoroborates. (C) 2009 Elsevier Ltd. All rights reserved.
Iron trichloride promoted hydrolysis of potassium organotrifluoroborates
作者:David W. Blevins、Min-Liang Yao、Li Yong、George W. Kabalka
DOI:10.1016/j.tetlet.2011.09.140
日期:2011.12
In the presence of iron trichloride, the hydrolysis of potassium organotrifluoroborates occurs smoothly at room temperature to afford the corresponding organoboronic acids in good to excellent yields. The hydrolysis is effective for aryltrifluoroborates as well as alkenyl- and alkyl-trifluoroborates.
Stereochemistry–activity relationship of orally active tetralin S1P agonist prodrugs
作者:Bin Ma、Kevin M. Guckian、Edward Yin-Shiang Lin、Wen-Cherng Lee、Daniel Scott、Gnanasambandam Kumaravel、Timothy L. Macdonald、Kevin R. Lynch、Cheryl Black、Sowmya Chollate、Kyungmin Hahm、Gregg Hetu、Ping Jin、Yi Luo、Ellen Rohde、Anthony Rossomando、Robert Scannevin、Joy Wang、Chunhua Yang
DOI:10.1016/j.bmcl.2010.02.006
日期:2010.4
Modifying FTY720, an immunosuppressant modulator, led to a new series of well phosphorylated tetralin analogs as potent S1P1 receptor agonists. The stereochemistry effect of tetralin ring was probed, and (-)(R)-2-amino-2-((S)-6-octyl-1,2,3,4-tetrahydronaphthalen-2-yl)propan-1-ol was identified as a good SphK2 substrate and potent S1P1 agonist with good oral bioavailability. (C) 2010 Elsevier Ltd. All rights reserved.