e.g. Filippa Pettersson or Cancer Res. 75(6) , 1102-12, (2015) or 10.1002/anie.201600521
Stereocontrolled synthesis of E-homoallylic sulfides with 1, 4, 5 related chiral centres using the [2, 3] sigmatropic rearrangement of sulfonium ylides
RC Hartley, IC Richards, S Warren
Index: Hartley, Richard C.; Richards, Ian C.; Warren, Stuart Journal of the Chemical Society - Perkin Transactions 1, 1996 , # 4 p. 359 - 376
E-Homoallylic sulfides with 1, 4, 5 related chiral centres have been synthesised in a stereocontrolled way. An aldol condensation sets up the stereochemistry. Lactonisation with 1, 2 arylsulfanyl migration followed by reduction and sulfur-assisted dehydration converts the aldols stereospecifically into allylic sulfides with 1, 2 related chiral centres. Sulfonium salts are generated from the allylic sulfides at low temperature, and are deprotonated to ...