662168-63-0Relevant academic research and scientific papers
Total syntheses of amphidinolides T1 and T4 via catalytic, stereoselective, reductive macrocyclizations
Colby, Elizabeth A.,O'Brien, Karen C.,Jamison, Timothy F.
, p. 4297 - 4307 (2007/10/03)
Described in this work are total syntheses of amphidinolides T1 and T4 using two nickel-catalyzed reductive coupling reactions of alkynes, with an epoxide in one case (intermolecular) and with an aldehyde in another (intramolecular). The latter was used t
Synthesis of Amphidinolide T1 via Catalytic, Stereoselective Macrocyclization
Colby, Elizabeth A.,O'Brien, Karen C.,Jamison, Timothy F.
, p. 998 - 999 (2007/10/03)
Two nickel-catalyzed reductive coupling reactions of alkynes were instrumental in a modular, stereoselective synthesis of amphidinolide T1 (1). The C13-C21 fragment was prepared from two simple starting materials that were joined in a catalytic alkyne-epo
