198493-28-6Relevant articles and documents
Asymmetric synthesis of the cholesteryl ester transfer protein inhibitor torcetrapib
Damon, David B.,Dugger, Robert W.,Hubbs, Stephen E.,Scott, Jill M.,Scott, Robert W.
, p. 472 - 480 (2006)
Previously our group reported synthetic efforts used to synthesize kilogram quantities of the cholesteryl ester transfer protein (CETP) inhibitor torcetrapib, 1, via a mid-stage resolution. This account describes research conducted to develop an asymmetri
Synthesis of homochiral N-Boc-β-aminoaldehydes from N-Boc-β-aminonitriles
Toujas, Jean-Louis,Jost, Eric,Vaultier, Michel
, p. 713 - 718 (2007/10/03)
Enantiopure N-Boc-β-aminoaldehydes are efficiently prepared in good yields from N-Boc-β-aminonitriles by reduction of the nitrile function with diisobutylaluminium hydride (DIBAL-H) - Keywords: β-aminoaldehyde; β-aminonitrile; α-aminoacid; homochiral; enantiomeric excess; reduction; DIBAL-H