Bornan

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Bornan
Skeletal formula
Ball-and-stick model
Nazivi
IUPAC naziv
(1S,4S)-1,7,7-trimetilbiciklo[2.2.1]heptan
Identifikacija
PubChem[1][2] 92108
Jmol-3D slike Slika 1
Svojstva
Molekulska formula C10H18
Molarna masa 138.24992
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa).
ДаY verifikuj (šta je ДаYНеН ?)
Reference infokutije

Bornan (kamfan) je jedinjenje koje je blisko srodno sa norbornanima.[3]

Biosinteza[уреди]

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[уреди]


Reference[уреди]

  1. 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. doi:10.1016/j.drudis.2010.10.003. PMID 20970519.  edit
  2. 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. 
  3. Clayden, Jonathan; Greeves, Nick; Warren, Stuart; Wothers, Peter (2001). Organic Chemistry (I изд.). Oxford University Press. ISBN 978-0-19-850346-0. 
  4. 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. 

Literatura[уреди]