- Stereoselective Synthesis and Evaluation of C6-Substituted 5a-Carbasugar Analogues of SL0101 as Inhibitors of RSK1/2
-
A convergent synthesis of 5a-carbasugar analogues of the n-Pr-variant of SL0101 is described. The analogues were synthesized in an effort to find compounds with potent in vivo efficacy in the inhibition of p90 ribosomal s6 kinase (RSK1/2). The synthesis derived the desired C-4 L-rhamnose stereochemistry from quinic acid and used a highly selective cuprate addition, NaBH4 reduction, Mitsunobu inversion, and alkene dihydroxylation to install the remaining stereochemistry. A Pd-catalyzed cyclitolization stereoselectively installed the aglycon at the anomeric position. The analogues were evaluated as RSK1/2 inhibitors and found to have 3- to 6-fold improved activity.
- Li, Mingzong,Li, Yu,Ludwik, Katarzyna A.,Sandusky, Zachary M.,Lannigan, Deborah A.,O’Doherty, George A.
-
p. 2410 - 2413
(2017/05/12)
-
- A stereoselective approach to functionalized cyclohexenones
-
A catalytic enantioselective approach to 4-hydroxy-6-methylcyclohex-2- enones is presented herein. The stereogenic information is generated through a copper-catalyzed 1,4-addition to p-benzoquinone monoketal using a chiral, BINOL-based (BINOL = 1,1′-bi-2-
- Meister, Anne C.,Sauter, Paul F.,Braese, Stefan
-
p. 7110 - 7116
(2013/11/06)
-
- Synthesis of carbasugar C-1 phosphates via Pd-catalyzed cyclopropanol ring opening
-
(Chemical Equation Presented) The stereoselective syntheses of 2,3-dideoxy-4-oxo-5a-carba-α-D-rhamnopyanose 1-phosphate, 2,3-dideoxy-5a-carba-α-D-rhamnopyranose 1-phosphate, 5a-carba-α-D- rhamnopyranose 1-phosphate, 5a-carba-α-D-digitoxopyranose 1-phosphate, and 5a-carba-α-L-rhamnopyranose 1-phosphate have been achieved from D-quinic acid. The routes rely upon a Simmons-Smith cyclopropanation and diastereospecific ring opening of cyclopropanol under Pd/C hydrogenation condition to set up the α-methyl ketone. A sequence of diastereoselective reduction, dihydroxylation, and/or Myers' reductive 1,3-rearrangement were used to install the desired stereochemistry.
- Shan, Mingde,O'Doherty, George A.
-
supporting information; experimental part
p. 3381 - 3384
(2009/05/11)
-
- Synthesis of cyclitols via cyclopropanation/palladium-catalyzed ring opening
-
The stereoselective syntheses of three cyclitols, 5a-carba-α-D- rhamnopyranose, 5a-carba-β-D-digitoxopyranose, and 5a-carba-α-L- rhamnopyranose, have been achieved. The routes rely upon a Simmons-Smith cyclopropanation and diastereospecific ring opening of cyclopropanol under Pd/C hydrogenation conditions to prepare the α-methyl ketone. A sequence of diastereoselective reduction, dihydroxylation, and/or Myers' reductive 1,3-rearrangement were used to install the desired stereochemistry. Georg Thieme Verlag Stuttgart.
- Shan, Mingde,O'Doherty, George A.
-
experimental part
p. 3171 - 3179
(2009/04/07)
-