77564-45-5Relevant academic research and scientific papers
SYNTHESIS OF TREE STEREOISOMERIC FORMS OF 2,8- DIMETHYL-1,7-DIOXASPIROUNDECANE, THE MAIN COMPONENT OF THE CEPHALIC SECRETION OF ANDRENA WILKELLA
Mori, Kenji,Tanida, Kaichi
, p. 3221 - 3225 (2007/10/02)
Three stereoisomers of 2,8-dimethyl-1,7-dioxaspiroundecane were synthesized from acetoacetic ester by utilizing its yeast reduction and dianion alkylation.
SYNTHESIS OF THREE STEREOISOMERIC FORMS OF 2,8-DIMETHYL-1,7-DIOXASPIROUNDECANE, THE MAIN COMPONENT OF THE CEPHALIC SECRETION OF ANDRENA WILKELLA
Mori, Kenji,Tanida, Kaichi
, p. 1171 - 1174 (2007/10/02)
Three stereoisomers of 2,8-dimethyl-1,7-dioxaspiroundecane with defined stereochemistry at C-2 and C-8 were synthesized utilizing yeast reduction and dianion alkylation of ethyl acetoacetate.
