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Ring Closing Metathesis Approach for the Synthesis of o ‐Terphenyl Derivatives
Author(s) -
Karmakar Shilpi,
Mandal Tirtha,
Dash Jyotirmayee
Publication year - 2019
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201900988
Subject(s) - chemistry , triphenylene , terphenyl , metathesis , ring closing metathesis , benzil , aromatization , salt metathesis reaction , stereochemistry , organic chemistry , molecule , polymerization , catalysis , polymer
A linear synthesis of o ‐terphenyl derivatives has been delineated using ring closing metathesis (RCM) as the key step. In this approach, benzil derivatives upon allyl Grignard addition provides diphenyl‐1,2‐diallyl dihydroxy derivatives which undergo ring closing metathesis to afford tetrahydro terphenyl derivatives. Aromatization‐driven dehydration then leads to a diverse set of electron rich and electron deficient o ‐terphenyls. Furthermore, oxidative coupling of electron rich o ‐terphenyls provides the corresponding triphenylene derivatives.
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