1443040-62-7Relevant articles and documents
Asymmetric Iterative Hydration of Polyene Strategy to Cryptocaryols A and B
Hunter, Thomas J.,Wang, Yanping,Zheng, Jiamin,O'Doherty, George A.
, p. 1700 - 1710 (2016/05/24)
The development of two iterative asymmetric hydration approaches to the synthesis of all syn- and syn/anti/syn-1,3,5,7-tetraol motifs is described. These pseudo-symmetric products are synthetic precursors for 1,3-hexol products. The utility of the route to the all syn-1,3,5,7-tetraol diastereoisomer was demonstrated with its use in the synthesis of cryptocaryols A and B, as well as, stereoisomers.
Cryptocaryol Structure-Activity Relationship Study of Cancer Cell Cytotoxicity and Ability to Stabilize PDCD4
Cuccarese, Michael F.,Wang, Yanping,Beuning, Penny J.,O'Doherty, George A.
, p. 522 - 526 (2014/06/09)
The synthetic cryptocaryols A and B and a series of their analogues have been evaluated for their cytotoxicity and their ability to stabilize the tumor suppressor PDCD4. Cytotoxicities in the 3 to 30 μM range were found. Both the cytotoxicity and PDCD4 stabilizing ability were tolerant of large stereochemical changes to the molecule. Co-dosing studies with cryptocaryols A and B and several known cancer drugs showed no measuable enhancement in cancer drug cytotoxicity.
Cryptocaryols A and B: Total syntheses, stereochemical revision, structure elucidation, and structure-activity relationship
Wang, Yanping,O'Doherty, George A.
, p. 9334 - 9337 (2013/07/25)
The first total syntheses and structural elucidation of cryptocaryol A and cryptocaryol B were achieved in 23 and 25 linear steps, respectively. The synthesis relied on the use of a key pseudo-Cs symmetric pentaol intermediate, which in a stere