[EN] 4-HYDROXYBUTYRIC ACID ANALOGS<br/>[FR] ANALOGUES DE L'ACIDE 4-HYDROXYBUTYRIQUE
申请人:CONCERT PHARMACEUTICALS INC
公开号:WO2010124046A1
公开(公告)日:2010-10-28
This invention relates to novel derivatives of 4-hydroxybutyric acid and prodrugs thereof, and pharmaceutically acceptable salts of the foregoing. This invention also provides pharmaceutical compositions comprising a compound of this invention and the use of such compositions in methods of treating narcolepsy, fibromyalgia, other disorders or conditions that are beneficially treated by improving nocturnal sleep or by administering sodium oxybate.
[EN] 4-HYDROXYBUTYRIC ACID DEUTERATED ANALOGS<br/>[FR] ANALOGUES DEUTÉRÉS DE L'ACIDE 4-HYDROXYBUTYRIQUE
申请人:CONCERT PHARMACEUTICALS INC
公开号:WO2012112492A1
公开(公告)日:2012-08-23
This invention relates to novel derivatives of 4-hydroxybutyric acid and prodrugs thereof, and pharmaceutically acceptable salts of the foregoing. This invention also provides pharmaceutical compositions comprising a compound of this invention and the use of such compositions in methods of treating narcolepsy, fibromyalgia, other disorders or conditions that are beneficially treated by improving nocturnal sleep or by administering sodium oxybate.
GUTMAN, A. L.;CAMPBELL, J. B., J. LABELLED COMPOUNDS AND RADIOPHARM., 1985, 22, N 7, 649-656
作者:GUTMAN, A. L.、CAMPBELL, J. B.
DOI:——
日期:——
GUTMAN, A. L., SYNTH. COMMUN., 1985, 15, N 5, 459-462
作者:GUTMAN, A. L.
DOI:——
日期:——
Use of Deuterium Labeling Studies to Determine the Stereochemical Outcome of Palladium Migrations during an Asymmetric Intermolecular Heck Reaction
作者:Bronwen M. M. Wheatley、Brian A. Keay
DOI:10.1021/jo071119u
日期:2007.9.1
[GRAPHICS]A series of deuterium labeling experiments showed that Pd migrations during an intermolecular asymmetric Heck reaction between phenyl triflate and various deuterated 2,3-dihydrofurans (2b, 2c, 2d, 2e) occurs exclusively by either syn-1,2-dyotropic shifts or a syn-chain-walking mechanism; no evidence was observed to support anti-1,2-dyotropic shifts or anti-beta-H Pd eliminations during the formation of 6 and 7.