Mary T Fletcher, Basilis E Mazomenos, John H Georgakopoulos, Maria A Konstantopoulou, Barry J Wood, James J De Voss, William Kitching
Index: Chem. Commun. (Camb.) (12) , 1302-3, (2002)
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The demonstration that both oxygen atoms of 1,7-dioxaspiro[5.5]undecane (1), the sex-pheromone of the female olive fly, originate from dioxygen, strongly implicates monooxygenase mediated processes in assembly of (1), and reveals unexpected complexity in the formation of its nine-carbon precursor.
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
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1,7-DIOXASPIRO[5.5]UNDECANE
CAS:180-84-7 |
C9H16O2 |
|
Spiroacetal biosynthesis: (+/-)-1,7-dioxaspiro[5.5]undecane ...
2005-03-17 [Org. Lett. 7(6) , 1173-6, (2005)] |
|
Non-covalent interactions in the crystallization of the enan...
2001-06-01 [Acta Crystallogr. B 57(Pt 3) , 399-409, (2001)] |
|
Analyzing diurnal and age-related pheromone emission of the ...
2012-08-01 [J. Chem. Ecol. 38(8) , 1036-41, (2012)] |
|
Inclusion of the main pheromone component of Dacus oleae, 1,...
1996-11-15 [Acta Crystallogr. C 52 ( Pt 11) , 2932-6, (1996)] |
|
Energetics of oxaspirocycle prototypes: 1,7-dioxaspiro[5.5]u...
2006-11-24 [J. Org. Chem. 71(24) , 9212-6, (2006)] |
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![1,7-DIOXASPIRO[5.5]UNDECANE Structure](http://hg.y866.cn/chemical/lib/image/caspic/490/180-84-7.png)