SYNTHESIS OF TREE STEREOISOMERIC FORMS OF 2,8- DIMETHYL-1,7-DIOXASPIROUNDECANE, THE MAIN COMPONENT OF THE CEPHALIC SECRETION OF ANDRENA WILKELLA

DOI: 10.1016/S0040-4020(01)98857-X

Source and publish data:

Tetrahedron p. 3221 - 3225 (1981)

Update date:2022-09-26

Topics:

Authors:

Mori, Kenji

Tanida, Kaichi

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Article abstract of DOI:10.1016/S0040-4020(01)98857-X

Three stereoisomers of 2,8-dimethyl-1,7-dioxaspiro<5,5>undecane were synthesized from acetoacetic ester by utilizing its yeast reduction and dianion alkylation.

Full text of DOI:10.1016/S0040-4020(01)98857-X

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