Bornan
| |||
| Nazivi | |||
|---|---|---|---|
| IUPAC naziv
(1S,4S)-1,7,7-trimetilbiciklo[2.2.1]heptan
| |||
| Identifikacija | |||
3D model (Jmol)
|
|||
| |||
| Svojstva | |||
| C10H18 | |||
| Molarna masa | 138,24992 | ||
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa). | |||
 verifikuj (šta je   ?)
| |||
| Reference infokutije | |||
Bornan (kamfan) je jedinjenje koje je blisko srodno sa norbornanima.[3]
Biosinteza[uredi | uredi izvor]
Bornan se formira tokom biosinteze kamfora iz geranil pirofosfata, putem ciklizacije linaloil pirofosfata do bornil pirofosfata.[4]
Biosynthesis of camphor from geranyl pyrophosphate
Vidi još[uredi | uredi izvor]
Reference[uredi | uredi izvor]
- ^ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.
- ^ Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
- ^ Clayden, Jonathan; Greeves, Nick; Warren, Stuart; Wothers, Peter (2001). Organic Chemistry (I изд.). Oxford University Press. ISBN 978-0-19-850346-0.
- ^ Rodney Croteau, Frank Karp (1979). „Biosynthesis of monoterpenes: Hydrolysis of bornyl pyrophosphate, an essential step in camphor biosynthesis, and hydrolysis of geranyl pyrophosphate, the acyclic precursor of camphor, by enzymes from sage (Salvia officinalis)”. Archives of Biochemistry and Biophysics. 198 (2): 523—532. PMID 42357. doi:10.1016/0003-9861(79)90527-7.