Cascade Reaction of 2,3-Naphthalenediol with Benzene in the Presence of Aluminum Halides Full article
| Journal |
Tetrahedron Letters
ISSN: 0040-4039 |
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| Output data | Year: 2019, Volume: 60, Number: 12, Pages: 857-859 Pages count : 3 DOI: 10.1016/j.tetlet.2019.02.026 | ||||||||
| Tags | Naphthols; Superelectrophilic activation; Electrophilic aromatic substitution; Ionic reduction | ||||||||
| Authors |
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| Affiliations |
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Funding (1)
| 1 | Federal Agency for Scientific Organizations | 0303-2016-0006 (V.44.1.6) |
Abstract:
2,3-Naphthalenediol on superelectrophilic activation with aluminium halides smoothly reacts with benzene to give 4-((3-phenyl-1H-inden-1-yl)methyl)benzene-1,2-diol, which in turn undergoes intramolecular cyclization to form 5,10-methano-5-phenyldibenzo[a,d]cycloheptane-2,3-diol. The mechanistic aspects of these unusual transformations are discussed.
Cite:
Zhu Z.
, Salnikov G.E.
, Koltunov K.Y.
Cascade Reaction of 2,3-Naphthalenediol with Benzene in the Presence of Aluminum Halides
Tetrahedron Letters. 2019. V.60. N12. P.857-859. DOI: 10.1016/j.tetlet.2019.02.026 WOS Scopus РИНЦ ANCAN OpenAlex
Cascade Reaction of 2,3-Naphthalenediol with Benzene in the Presence of Aluminum Halides
Tetrahedron Letters. 2019. V.60. N12. P.857-859. DOI: 10.1016/j.tetlet.2019.02.026 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
| Submitted: | Jan 16, 2019 |
| Accepted: | Feb 13, 2019 |
| Published online: | Feb 14, 2019 |
| Published print: | Mar 1, 2019 |
Identifiers:
| Web of science: | WOS:000461535700010 |
| Scopus: | 2-s2.0-85061628865 |
| Elibrary: | 38669438 |
| Chemical Abstracts: | 2019:350051 |
| Chemical Abstracts (print): | 170:388265 |
| OpenAlex: | W2911927543 |