445423-05-2Relevant academic research and scientific papers
The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: The CD-spiroacetal segment
Paterson, Ian,Coster, Mark J.,Chen, David Y.-K.,Gibson, Karl R.,Wallace, Debra J.
, p. 2410 - 2419 (2007/10/03)
Stereocontrolled syntheses of the C16-C28 CD-spiroacetal subunit of altohyrtin A/spongistatin 1 (1), relying on kinetic and thermodynamic control of the spiroacetal formation, are described. The kinetic control approach resulted in a slight preference (60: 40) for the desired spiroacetal isomer. The thermodynamic approach allowed ready access to the desired spiroacetal 2 by acid-promoted equilibration, Chromatographic separation of the C23 epimers and resubjection of the undesired isomer to the equilibration conditions. This scalable synthetic sequence provided multi-gram quantities of 2, thus enabling the successful completion of the total synthesis of altohyrtin A/spongistatin 1, as reported in Part 4 of this series. The Royal Society of Chemistry 2005.
Total synthesis of altohyrtin A (spongistatin 1): An alternative synthesis of the CD-spiroacetal subunit
Paterson, Ian,Coster, Mark J
, p. 3285 - 3289 (2007/10/03)
The CD-spiroacetal containing C16-C28 subunit 2, as used in the total synthesis of the potent cytotoxic macrolide, altohyrtin A (spongistatin 1), was prepared by an alternative route using substrate-based stereocontrol in the two ald
