884345-36-2Relevant academic research and scientific papers
The evolution of a stereoselective synthesis of the C1-C16 fragment of bryostatins
Ball, Matthew,Baron, Anne,Bradshaw, Ben,Dumeunier, Rapha?l,O'Brien, Matthew,Thomas, Eric J.
, p. 9650 - 9681 (2016/10/22)
The development of a synthesis of the C1-C16 fragment of bryostatins in which the key step is a stereoselective oxy-Michael reaction used to assemble the cis-2,6-disubstituted tetrahydropyran with the exocyclic alkene already installed, is described. Foll
A preliminary evaluation of a metathesis approach to bryostatins
Ball, Matthew,Bradshaw, Benjamin J.,Dumeunier, Rapha?l,Gregson, Thomas J.,MacCormick, Somhairle,Omori, Hiroki,Thomas, Eric J.
, p. 2223 - 2227 (2007/10/03)
Preliminary investigations into the synthesis of bryostatins using ring-closing metathesis to form the C(16)-C(17) double bond led to a synthesis of the bryostatin analogue 51; precursors 26 and 52, which possess the geminal dimethyl group at C-18, did no
