1003890-41-2Relevant academic research and scientific papers
A phosphate tether-mediated, one-pot, sequential ring-closing metathesis/cross-metathesis/chemoselective hydrogenation protocol
Venukadasula, Phanindra K. M.,Chegondi, Rambabu,Suryn, Gregory M.,Hanson, Paul R.
, p. 2634 - 2637 (2012/07/31)
A versatile three-step, one-pot, sequential reaction protocol involving ring-closing metathesis, cross-metathesis, and chemoselective hydrogenation is reported. This phosphate tether-mediated process occurs without intermediate isolation, is chemoselectiv
Total synthesis of dolabelide C: A phosphate-mediated approach
Hanson, Paul R.,Chegondi, Rambabu,Nguyen, John,Thomas, Christopher D.,Waetzig, Joshua D.,Whitehead, Alan
, p. 4358 - 4370 (2011/07/06)
The first synthesis of dolabelide C (1), a cytotoxic marine macrolide, is reported utilizing a phosphate tether-mediated approach. Bicyclic phosphates (S,S,SP)-5 and (R,R,RP)-5 serve as the central building blocks for the constructio
A multifaceted phosphate tether: Application to the C1-C14 subunit of dolabelides A-D
Waetzig, Joshua D.,Hanson, Paul R.
, p. 109 - 112 (2008/09/16)
A phosphate tether approach to the C1-14 subunit of dolabelide is described. The phosphate tether serves a multifaceted role mediating several processes, including (i) diastereotopic differentiation via RCM, (ii) selective CM by imparting Type III behavior to the exocyclic olefin, (iii) regioselective hydrogenation, and (iv) regioselective Pd(0)-catalyzed reductive opening of the bicyclic phosphate. Overall, this strategy uses orthogonal protecting- and leaving-group properties innate to phosphate esters to rapidly assembly the titled subunit.
