TY - JOUR
T1 - An Efficient Synthesis of Dibenzo[a,l]tetracene and Dibenzo[a,j]tetracene and Their Identification in a Coal Tar Extract
AU - Ramisetti, Srinivasa R.
AU - Oña-Ruales, Jorge O.
AU - Wise, Stephen A.
AU - Amin, Shantu
AU - Sharma, Arun K.
N1 - Publisher Copyright:
© 2017, © 2017 Taylor & Francis Group, LLC.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - An efficient synthesis of potentially carcinogenic dibenzo[a,l]tetracene 1 and dibenzo[a,j]tetracene 2 has been developed and the synthetic standards were used to establish their environmental presence. The synthesis involves Diels–Alder reaction of in situ generated ortho-quinodimethane with phenanthrene-1,4-dione, followed by reductive aromatization as key steps. This synthetic strategy resulted in good overall yield and the mixture of 1 and 2 is easily separable by reversed-phase liquid chromatography (RP-LC). Compounds 1 and 2 were identified in a complex mixture of polycyclic aromatic hydrocarbons from coal tar (Standard Reference Material 1597a) and thus could be potential environmental hazards.
AB - An efficient synthesis of potentially carcinogenic dibenzo[a,l]tetracene 1 and dibenzo[a,j]tetracene 2 has been developed and the synthetic standards were used to establish their environmental presence. The synthesis involves Diels–Alder reaction of in situ generated ortho-quinodimethane with phenanthrene-1,4-dione, followed by reductive aromatization as key steps. This synthetic strategy resulted in good overall yield and the mixture of 1 and 2 is easily separable by reversed-phase liquid chromatography (RP-LC). Compounds 1 and 2 were identified in a complex mixture of polycyclic aromatic hydrocarbons from coal tar (Standard Reference Material 1597a) and thus could be potential environmental hazards.
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U2 - 10.1080/10406638.2017.1362013
DO - 10.1080/10406638.2017.1362013
M3 - Article
AN - SCOPUS:85029427479
SN - 1040-6638
VL - 40
SP - 88
EP - 98
JO - Polycyclic Aromatic Compounds
JF - Polycyclic Aromatic Compounds
IS - 1
ER -