Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides

Standard

Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides. / Zhu, Zhongwei; Salnikov, George E.; Koltunov, Konstantin Yu.

в: Tetrahedron Letters, Том 60, № 12, 21.03.2019, стр. 857-859.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Zhu, Z, Salnikov, GE & Koltunov, KY 2019, 'Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides', Tetrahedron Letters, Том. 60, № 12, стр. 857-859. https://doi.org/10.1016/j.tetlet.2019.02.026

APA

Zhu, Z., Salnikov, G. E., & Koltunov, K. Y. (2019). Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides. Tetrahedron Letters, 60(12), 857-859. https://doi.org/10.1016/j.tetlet.2019.02.026

Vancouver

Zhu Z, Salnikov GE, Koltunov KY. Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides. Tetrahedron Letters. 2019 март 21;60(12):857-859. doi: 10.1016/j.tetlet.2019.02.026

Author

Zhu, Zhongwei ; Salnikov, George E. ; Koltunov, Konstantin Yu. / Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides. в: Tetrahedron Letters. 2019 ; Том 60, № 12. стр. 857-859.

BibTeX

@article{8e452349ab92477cbe42f83319313a89,

title = "Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides",

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.",

keywords = "Electrophilic aromatic substitution, Ionic reduction, Naphthols, Superelectrophilic activation, HCL, NAPHTHALENEDIOLS, CYCLOHEXANE, CONDENSATION, CHLOROALUMINATE",

author = "Zhongwei Zhu and Salnikov, {George E.} and Koltunov, {Konstantin Yu}",

note = "Publisher Copyright: {\textcopyright} 2019 Elsevier Ltd",

year = "2019",

month = mar,

day = "21",

doi = "10.1016/j.tetlet.2019.02.026",

language = "English",

volume = "60",

pages = "857--859",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "12",

}

RIS

TY - JOUR

T1 - Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides

AU - Zhu, Zhongwei

AU - Salnikov, George E.

AU - Koltunov, Konstantin Yu

PY - 2019/3/21

Y1 - 2019/3/21

N2 - 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.

AB - 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.

KW - Electrophilic aromatic substitution

KW - Ionic reduction

KW - Naphthols

KW - Superelectrophilic activation

KW - HCL

KW - NAPHTHALENEDIOLS

KW - CYCLOHEXANE

KW - CONDENSATION

KW - CHLOROALUMINATE

UR - http://www.scopus.com/inward/record.url?scp=85061628865&partnerID=8YFLogxK

U2 - 10.1016/j.tetlet.2019.02.026

DO - 10.1016/j.tetlet.2019.02.026

M3 - Article

AN - SCOPUS:85061628865

VL - 60

SP - 857

EP - 859

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 12

ER -

ID: 18561048