180-84-7Relevant articles and documents
Pherome syntheses - Model reactions for the synthesis of polyether antibiotics
Ireland,Habich
, p. 1418 - 1427 (1981)
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A simple enantioselective synthesis of (R)- and (S)-1,7-dioxaspiro[5.5]undecane via intramolecular asymmetric oxyselenenylation: A new route to optically active spiroketals
Uchiyama, Masahiko,Oka, Masako,Harai, Satohide,Ohta, Akihiro
, p. 1931 - 1934 (2001)
Both enantiomers of 1,7-dioxaspiro[5.5]undecane, the major pheromone components of the olive fruit fly (Bactrocea oleae), have been synthesized by using a new method based on the intramolecular asymmetric oxyselenenylation of 4-(3,4-dihydro-2H-pyran-6-yl)butan-1-ol.
A new short synthesis of (±)-olean through cross metathesis
Kranidiotis, Nektarios S.,Grammatoglou, Constantinos E.,Gallos, John K.
, p. 1441 - 1444 (2018/08/29)
A new synthesis of (±)-1,7-dioxaspiro[5.5]undecane (olean), the olive fruit fly pheromone, utilizing the cross-metathesis reaction as the key-step, is reported.
CHIRAL IMIDODIPHOSPHATES AND DERIVATIVES THEREOF
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, (2013/07/25)
The invention relates to chiral imidodiphosphates and derivatives thereof having the general formula I, The compounds are suitable as chiral Br?nsted acid catalysts, phase-transfer catalysts, chiral anions for organic salts, metal salts or metal complexes for catalysis.