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Articles • J. Braz. Chem. Soc. 12 (3) • June 2001 • https://doi.org/10.1590/S0103-50532001000300009   copy

The stereochemistry of the Nozaki-Hiyama-Kishi reaction and the construction of 10-membered lactones. The enantioselective total synthesis of (-)-decarestrictine D

Authorship SCIMAGO INSTITUTIONS RANKINGS

The use of the intramolecular Nozaki-Hiyama-Kishi reaction to construct 10-membered lactones is described. The influence of the nature of the protecting groups at C4 and C5 on the stereochemistry of the newly formed stereogenic center at C7 was investigated. The utility of this methodology has been demonstrated in the stereoselective total synthesis of (-)-decarestrictine D from 1,3-propanediol and polyhydroxybutyrate (PHB) in 13 steps and 6.3% overall yield.

decarestrictine D; decanolide; Nozaki-Hiyama-Kishi reaction; lactone

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