Anionic 1,4 O→C silyl rearrangements

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Anionic 1,4 O→C silyl rearrangements. / Rücker, Christoph.
in: Tetrahedron Letters, Jahrgang 25, Nr. 39, 1984, S. 4349-4352.

Publikation: Beiträge in ZeitschriftenZeitschriftenaufsätzeForschungbegutachtet

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Rücker C. Anionic 1,4 O→C silyl rearrangements. Tetrahedron Letters. 1984;25(39):4349-4352. doi: 10.1016/S0040-4039(01)81435-0

Bibtex

@article{84845377b82242ceab163290f8f217f3,
title = "Anionic 1,4 O→C silyl rearrangements",
abstract = "γ-Silyloxy-alkyl phenyl thioethers are transformed into γ-silylalcohols by treatment with lithium di-tert-butylbiphenyl.",
keywords = "Chemistry",
author = "Christoph R{\"u}cker",
note = "Funding Information: Acknowledgement. Support by the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen",
year = "1984",
doi = "10.1016/S0040-4039(01)81435-0",
language = "English",
volume = "25",
pages = "4349--4352",
journal = "Tetrahedron Letters",
issn = "1873-3581",
publisher = "Elsevier B.V.",
number = "39",

}

RIS

TY - JOUR

T1 - Anionic 1,4 O→C silyl rearrangements

AU - Rücker, Christoph

N1 - Funding Information: Acknowledgement. Support by the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen

PY - 1984

Y1 - 1984

N2 - γ-Silyloxy-alkyl phenyl thioethers are transformed into γ-silylalcohols by treatment with lithium di-tert-butylbiphenyl.

AB - γ-Silyloxy-alkyl phenyl thioethers are transformed into γ-silylalcohols by treatment with lithium di-tert-butylbiphenyl.

KW - Chemistry

UR - http://www.scopus.com/inward/record.url?scp=0000603538&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(01)81435-0

DO - 10.1016/S0040-4039(01)81435-0

M3 - Journal articles

VL - 25

SP - 4349

EP - 4352

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 1873-3581

IS - 39

ER -

DOI