552289-40-4Relevant academic research and scientific papers
A unified strategy for enantioselective total synthesis of cladiellin and briarellin diterpenes: Total synthesis of briarellins E and F and the putative structure of alcyonin and revision of its structure assignment
Corminboeuf, Olivier,Overman, Larry E.,Pennington, Lewis D.
supporting information; experimental part, p. 5458 - 5470 (2009/12/06)
(Chemical Equation Presented) Enantioselective total syntheses of briarellin E (12) and briarellin F (13), as well as the structure originally proposed for the cladiellin diterpene alcyonin (10), have been realized. Comparison of the spectral data for synthetic 10, natural alcyonin, cladiellisin (33), and cladiellaperoxide (34), as well as chemical transformations of 10 and natural alcyonin, suggest that the structure of this coral metabolite is allylic peroxide 11. The unified approach detailed herein can be used to access both C4-deoxygenated and C4-oxygenated cladiellins and briarellins. The central step in these syntheses is acid-promoted condensation of (Z)-α,β- unsaturated aldehydes 17 with cyclohexadienyl diols 18 to form intermediates 16 incorporating the hexahydroisobenzofuran core and five stereocenters of these marine diterpenes (Scheme 1).
Enantioselective total synthesis of briarellins E and F: The first total syntheses of briarellin diterpenes
Corminboeuf, Olivier,Overman, Larry E.,Pennington, Lewis D.
, p. 6650 - 6652 (2007/10/03)
Enantioselective total syntheses of briarellin E (4) and briarellin F (5) have been achieved starting with (S)-(+)-carvone and (S)-(-)-glycidol. These total syntheses are the first of briarellin diterpenes. The central step in these syntheses is acid-prom
