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An efficient method of synthesis of isoxazolidine-fused β-lactams via base-promoted cyclization–ring opening of carbamoyl-spirocyclopropane isoxazolidines. / Tran, T.Q.; Savinkov, R.S.; Diev, V.V.; Starova, G.L.; Molchanov, A.P.

In: Tetrahedron, Vol. 69, No. 25, 2013, p. 5173-5177.

Research output: Contribution to journal › Article

Harvard

Tran, TQ, Savinkov, RS, Diev, VV, Starova, GL & Molchanov, AP 2013, 'An efficient method of synthesis of isoxazolidine-fused β-lactams via base-promoted cyclization–ring opening of carbamoyl-spirocyclopropane isoxazolidines', Tetrahedron, vol. 69, no. 25, pp. 5173-5177. https://doi.org/10.1016/j.tet.2013.04.054

APA

Tran, T. Q., Savinkov, R. S., Diev, V. V., Starova, G. L., & Molchanov, A. P. (2013). An efficient method of synthesis of isoxazolidine-fused β-lactams via base-promoted cyclization–ring opening of carbamoyl-spirocyclopropane isoxazolidines. Tetrahedron, 69(25), 5173-5177. https://doi.org/10.1016/j.tet.2013.04.054

Vancouver

Tran TQ, Savinkov RS, Diev VV, Starova GL, Molchanov AP. An efficient method of synthesis of isoxazolidine-fused β-lactams via base-promoted cyclization–ring opening of carbamoyl-spirocyclopropane isoxazolidines. Tetrahedron. 2013;69(25):5173-5177. https://doi.org/10.1016/j.tet.2013.04.054

Author

Tran, T.Q. ; Savinkov, R.S. ; Diev, V.V. ; Starova, G.L. ; Molchanov, A.P. / An efficient method of synthesis of isoxazolidine-fused β-lactams via base-promoted cyclization–ring opening of carbamoyl-spirocyclopropane isoxazolidines. In: Tetrahedron. 2013 ; Vol. 69, No. 25. pp. 5173-5177.

BibTeX

@article{cf4a490e371b4aff88c5ff6906d52d95,
title = "An efficient method of synthesis of isoxazolidine-fused β-lactams via base-promoted cyclization–ring opening of carbamoyl-spirocyclopropane isoxazolidines",
abstract = "1,3-Dipolar cycloadditions of dialkyl-substituted 2-benzylidenecyclopropane-1,1-dicarboxylates and a number of C-carbamoyl nitrones proceed with high efficiency and selectivity with the formation of single isomeric spiro[cyclopropane-1,4-isoxazolidine] cycloadduct. Obtained cycloadducts easily undergo cyclopropyl ring opening-cyclization to form new beta-lactams fused with isoxazolidine ring in high yields. (C) 2013 Elsevier Ltd. All rights reserved.",
author = "T.Q. Tran and R.S. Savinkov and V.V. Diev and G.L. Starova and A.P. Molchanov",
year = "2013",
doi = "10.1016/j.tet.2013.04.054",
language = "English",
volume = "69",
pages = "5173--5177",
journal = "Tetrahedron",
issn = "0040-4020",
publisher = "Elsevier",
number = "25",

}

RIS

TY - JOUR

T1 - An efficient method of synthesis of isoxazolidine-fused β-lactams via base-promoted cyclization–ring opening of carbamoyl-spirocyclopropane isoxazolidines

AU - Tran, T.Q.

AU - Savinkov, R.S.

AU - Diev, V.V.

AU - Starova, G.L.

AU - Molchanov, A.P.

PY - 2013

Y1 - 2013

N2 - 1,3-Dipolar cycloadditions of dialkyl-substituted 2-benzylidenecyclopropane-1,1-dicarboxylates and a number of C-carbamoyl nitrones proceed with high efficiency and selectivity with the formation of single isomeric spiro[cyclopropane-1,4-isoxazolidine] cycloadduct. Obtained cycloadducts easily undergo cyclopropyl ring opening-cyclization to form new beta-lactams fused with isoxazolidine ring in high yields. (C) 2013 Elsevier Ltd. All rights reserved.

AB - 1,3-Dipolar cycloadditions of dialkyl-substituted 2-benzylidenecyclopropane-1,1-dicarboxylates and a number of C-carbamoyl nitrones proceed with high efficiency and selectivity with the formation of single isomeric spiro[cyclopropane-1,4-isoxazolidine] cycloadduct. Obtained cycloadducts easily undergo cyclopropyl ring opening-cyclization to form new beta-lactams fused with isoxazolidine ring in high yields. (C) 2013 Elsevier Ltd. All rights reserved.

U2 - 10.1016/j.tet.2013.04.054

DO - 10.1016/j.tet.2013.04.054

M3 - Article

VL - 69

SP - 5173

EP - 5177

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 25

ER -

ID: 7389055