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Source: The Open Library

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1Natural products related to phenanthrene

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“Natural products related to phenanthrene” Metadata:

  • Title: ➤  Natural products related to phenanthrene
  • Author:
  • Language: English
  • Number of Pages: Median: 704
  • Publisher: Reinhold Pub. Corp.
  • Publish Date:
  • Publish Location: New York

“Natural products related to phenanthrene” Subjects and Themes:

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Access and General Info:

  • First Year Published: 1949
  • Is Full Text Available: Yes
  • Is The Book Public: No
  • Access Status: Borrowable

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Phenanthrene

Phenanthrene is a polycyclic aromatic hydrocarbon (PAH) with formula C14H10, consisting of three fused benzene rings. It is a colorless, crystal-like solid

Friedel–Crafts reaction

isomerization of 1-β-phenylethylcyclohexanol to the octahydro derivative of phenanthrene The Darzens–Nenitzescu synthesis of ketones (1910, 1936) involves the

Pyrene

Pyrene Names Preferred IUPAC name Pyrene Other names Benzo[def]phenanthrene Identifiers CAS Number 129-00-0 Y 3D model (JSmol) Interactive image Beilstein

Phenanthrenoid

Phenanthrenoids are chemical compounds formed with a phenanthrene backbone. These compounds occur naturally in plants, although they can also be synthesized

1-Hydroxyphenanthrene

1-Hydroxyphenanthrene is a phenanthrol and a human metabolite of phenanthrene that can be detected in urine of persons exposed to PAHs. It can also be

Diphenic acid

via the diazonium salt. It is the product of the microbial action on phenanthrene. The compound forms a variety of coordination polymers. It also exhibits

Benz(a)anthracene

Benz[a]anthracene Benzanthracene Benzanthrene 1,2-Benzanthracene Benzo[b]phenanthrene Tetracyclo[8.8.0.02,7.012,17]octadeca-1,3,5,7,9,11,13,15,17-nonaene[citation

Benzo(c)phenanthrene

Benzo[c]phenanthrene is a polycyclic aromatic hydrocarbon with the chemical formula C18H12. It is a white solid that is soluble in nonpolar organic solvents

Gonane

with a fully hydrogenated molecule of phenanthrene, hence the more descriptive name "perhydrocyclopenta[a]phenanthrene". The non-systematic version of the

Enyne metathesis

to a phenanthrene in scheme 3: The carbene is a tungsten carbonyl when used in stoichiometric amounts (1 equivalent) yields 41% of the phenanthrene 3.2