88818-17-1Relevant articles and documents
Toward the synthesis of spirastrellolide B: A synthesis of the C1-C23 subunit
Keaton, Katie A.,Phillips, Andrew J.
body text, p. 1083 - 1086 (2009/04/06)
A synthesis of the C1-C23 subunit of spirastrellolide B is described. The synthesis features two applications of a Kulinkovich-cyclopropanol ring-opening strategy for the coupling of esters with olefins to produce ketones.
Proof that the Absolute Configuration of Natural α-Lipoic Acid is R by the Synthesis of its Enantiomer from (S)-Malic Acid
Brookes, Michael H.,Golding, Bernard T.,Howes, David A.,Hudson, Alan T.
, p. 1051 - 1053 (2007/10/02)
The absolute configuration of natural (+)-α-lipoic acid is confirmed to be R by the synthesis of its enantiomer from (S)-malic acid.