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Reductive alkylation of beta-alkoxy aziridines: new route to substituted allylic amines

Research output: Contribution to Journal/Magazine › Journal article › peer-review

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Reductive alkylation of beta-alkoxy aziridines: new route to substituted allylic amines. / Rosser, Clare M.; Coote, Susannah C.; Kirby, Jonathan P. et al.
In: Organic Letters, Vol. 6, No. 26, 23.12.2004, p. 4817-4819.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Rosser, CM, Coote, SC, Kirby, JP, O'Brien, P & Caine, D 2004, 'Reductive alkylation of beta-alkoxy aziridines: new route to substituted allylic amines', Organic Letters, vol. 6, no. 26, pp. 4817-4819. https://doi.org/10.1021/ol048201l

APA

Rosser, C. M., Coote, S. C., Kirby, J. P., O'Brien, P., & Caine, D. (2004). Reductive alkylation of beta-alkoxy aziridines: new route to substituted allylic amines. Organic Letters, 6(26), 4817-4819. https://doi.org/10.1021/ol048201l

Vancouver

Rosser CM, Coote SC, Kirby JP, O'Brien P, Caine D. Reductive alkylation of beta-alkoxy aziridines: new route to substituted allylic amines. Organic Letters. 2004 Dec 23;6(26):4817-4819. doi: 10.1021/ol048201l

Author

Rosser, Clare M. ; Coote, Susannah C. ; Kirby, Jonathan P. et al. / Reductive alkylation of beta-alkoxy aziridines : new route to substituted allylic amines. In: Organic Letters. 2004 ; Vol. 6, No. 26. pp. 4817-4819.

Bibtex

@article{f1801d376de348619ae942fd7650bb9d,
title = "Reductive alkylation of beta-alkoxy aziridines: new route to substituted allylic amines",
abstract = "A new route to substituted cyclic allylic amines via the reductive alkylation of beta-alkoxy aziridines using excess alkyllithium reagents is described.",
keywords = "ALPHA-LITHIATION-REARRANGEMENT, EPOXIDES, REAGENTS, DESYMMETRIZATION, DERIVATIVES, CARBENOIDS, CHEMISTRY, OXIRANYL, ALCOHOLS, SYSTEMS",
author = "Rosser, {Clare M.} and Coote, {Susannah C.} and Kirby, {Jonathan P.} and Peter O'Brien and Darren Caine",
year = "2004",
month = dec,
day = "23",
doi = "10.1021/ol048201l",
language = "English",
volume = "6",
pages = "4817--4819",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "26",

}

RIS

TY - JOUR

T1 - Reductive alkylation of beta-alkoxy aziridines

T2 - new route to substituted allylic amines

AU - Rosser, Clare M.

AU - Coote, Susannah C.

AU - Kirby, Jonathan P.

AU - O'Brien, Peter

AU - Caine, Darren

PY - 2004/12/23

Y1 - 2004/12/23

N2 - A new route to substituted cyclic allylic amines via the reductive alkylation of beta-alkoxy aziridines using excess alkyllithium reagents is described.

AB - A new route to substituted cyclic allylic amines via the reductive alkylation of beta-alkoxy aziridines using excess alkyllithium reagents is described.

KW - ALPHA-LITHIATION-REARRANGEMENT

KW - EPOXIDES

KW - REAGENTS

KW - DESYMMETRIZATION

KW - DERIVATIVES

KW - CARBENOIDS

KW - CHEMISTRY

KW - OXIRANYL

KW - ALCOHOLS

KW - SYSTEMS

U2 - 10.1021/ol048201l

DO - 10.1021/ol048201l

M3 - Journal article

VL - 6

SP - 4817

EP - 4819

JO - Organic Letters

JF - Organic Letters

SN - 1523-7060

IS - 26

ER -