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@article{b552c3f507cd4364b12e6a4d0e3cede0,
title = "Synthesis of isoxazolopyrroloisoquinolines by intramolecular cyclizations of 5-(2-arylethyl)-6-hydroxytetrahydro-4H-pyrrolo[3,4-d]isoxazol-4-ones",
abstract = "5,8a,11a,11b-Tetrahydroisoxazolo[5′,4′:3,4]pyrrolo[2,1-a] isoquinolin-8(6H)-ones were prepared by intramolecular cyclization of 5-(2-arylethyl)-6-hydroxytetrahydro-4H-pyrrolo[3,4-d]isoxazol-4-ones in the presence of boron trifluoride diethyl etherate.",
keywords = "Pyrrolo[2,1-a]isoquinolines, Isoxazolopyrroloisoquinolines, Dihydroisoxazoles, Hydroxylactams, N-Acyliminium ion, Intramolecular cyclization",
author = "Stepakov, {Alexander V.} and Ledovskaya, {Maria S.} and Boitsov, {Vitaly M.} and Molchanov, {Alexander P.} and Kostikov, {Rafael R.} and Gurzhiy, {Vladislav V.} and Starova, {Galina L.}",
note = "Funding Information: This work was supported by the Russian Foundation for Basic Research (Project no. 12-03-01008-a ). We are grateful to Dr. Sergey Vyazmin and Dr. Elena Grinenko for recording IR spectra. ",
year = "2012",
month = oct,
day = "3",
doi = "10.1016/j.tetlet.2012.07.114",
language = "English",
volume = "53",
pages = "5414--5417",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier",
number = "40",

}

RIS

TY - JOUR

T1 - Synthesis of isoxazolopyrroloisoquinolines by intramolecular cyclizations of 5-(2-arylethyl)-6-hydroxytetrahydro-4H-pyrrolo[3,4-d]isoxazol-4-ones

AU - Stepakov, Alexander V.

AU - Ledovskaya, Maria S.

AU - Boitsov, Vitaly M.

AU - Molchanov, Alexander P.

AU - Kostikov, Rafael R.

AU - Gurzhiy, Vladislav V.

AU - Starova, Galina L.

N1 - Funding Information: This work was supported by the Russian Foundation for Basic Research (Project no. 12-03-01008-a ). We are grateful to Dr. Sergey Vyazmin and Dr. Elena Grinenko for recording IR spectra.

PY - 2012/10/3

Y1 - 2012/10/3

N2 - 5,8a,11a,11b-Tetrahydroisoxazolo[5′,4′:3,4]pyrrolo[2,1-a] isoquinolin-8(6H)-ones were prepared by intramolecular cyclization of 5-(2-arylethyl)-6-hydroxytetrahydro-4H-pyrrolo[3,4-d]isoxazol-4-ones in the presence of boron trifluoride diethyl etherate.

AB - 5,8a,11a,11b-Tetrahydroisoxazolo[5′,4′:3,4]pyrrolo[2,1-a] isoquinolin-8(6H)-ones were prepared by intramolecular cyclization of 5-(2-arylethyl)-6-hydroxytetrahydro-4H-pyrrolo[3,4-d]isoxazol-4-ones in the presence of boron trifluoride diethyl etherate.

KW - Pyrrolo[2,1-a]isoquinolines

KW - Isoxazolopyrroloisoquinolines

KW - Dihydroisoxazoles

KW - Hydroxylactams

KW - N-Acyliminium ion

KW - Intramolecular cyclization

UR - http://www.scopus.com/inward/record.url?scp=84865682354&partnerID=8YFLogxK

U2 - 10.1016/j.tetlet.2012.07.114

DO - 10.1016/j.tetlet.2012.07.114

M3 - Article

VL - 53

SP - 5414

EP - 5417

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 40

ER -

ID: 5334622