APPLICATION OF THE CARBONYL EPOXIDE REARRANGEMENT TO THE FORMATION OF DIOXABICYCLOALKANES AND ALKENES. SYNTHESIS OF THE MUS MUSCULUS PHEROMONE

DOI: 10.1016/S0040-4039(00)85095-9

Source and publish data:

Tetrahedron Letters p. 4909 - 4912 (1986)

Update date:2022-09-26

Topics:

Authors:

Wasserman, Harry H.

Wolff, Steven

Oku, Teruo

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Article abstract of DOI:10.1016/S0040-4039(00)85095-9

Acid-catalyzed intramolecular opening of epoxides by carbonyl groups provides a general stereocontrolled method for forming dioxabicyclo systems, including the (+/-)-Mus musculus pheromone and products corresponding to certain insect pheromones.

Full text of DOI:10.1016/S0040-4039(00)85095-9

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