STEREOCONTROLLED SYNTHESIS OF (RR)- AND (RS)-5-HYDROXY-2-METHYLHEXANOIC ACID LACTONES. PHEROMONE OF THE CARPENTER BEE VIA PALLADIUM-CATALYZED REACTIONS

DOI: 10.1016/S0040-4020(01)91414-0

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Tetrahedron p. 5761 - 5764 (1985)

Update date:2022-08-05

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Authors:

Baeckvall, J. E.

Bystroem, S. E.

Nystroem, J. E.

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Article abstract of DOI:10.1016/S0040-4020(01)91414-0

(E,Z)-2,4-Hexadiene was transformed to the lactone cis-1(>93percent cis)(pheromone of the carpenter bee) in a stereospecific reaction sequence via a Pd-catalyzed 1,4-acetoxychlorination.The same reaction sequence applied to (E,E)-2,4-hexadiene afforded th

Full text of DOI:10.1016/S0040-4020(01)91414-0

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Article Doi

STEREOCONTROLLED SYNTHESIS OF (R*R*)- AND (R*S*)-5-HYDROXY-2-METHYLHEXANOIC ACID LACTONES. PHEROMONE OF THE CARPENTER BEE VIA PALLADIUM-CATALYZED REACTIONS

DOI: 10.1016/S0040-4020(01)91414-0

Source and publish data: