Anionic 1,4 O→C silyl rearrangements

Christoph Rücker

doi:10.1016/S0040-4039(01)81435-0

Anionic 1,4 O→C silyl rearrangements

Research output: Journal contributions › Journal articles › Research › peer-review

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Anionic 1,4 O→C silyl rearrangements. / Rücker, Christoph.
In: Tetrahedron Letters, Vol. 25, No. 39, 1984, p. 4349-4352.

Research output: Journal contributions › Journal articles › Research › peer-review

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 -

Useful synthetic reagents derived from 1-triisopropylsilylpropyne and 1,3bis-[triisopropylsilyl]propyne, direct, stereoselective synthesis of either Z or E enynes

Corey, E. J. & Rücker, C., 1982, In: Tetrahedron Letters. 23, 7, p. 719-722 4 p.

Research output: Journal contributions › Journal articles › Research › peer-review

Comment on "nomenclature, Chemical Abstracts Service Numbers, Isomer Enumeration, Ring Strain, and Stereochemistry: What Does Any of This Have to Do with an International Chemical Disarmament and Nonproliferation Treaty?"

Rücker, C., Meringer, M. & Wassermann, A., 13.04.2021, In: Journal of Chemical Education. 98, 4, p. 1465-1467 3 p.

Research output: Journal contributions › Comments / Debate / Reports › Research

Octanol-Water Partition Coefficient Measurement by a Simple ¹H NMR Method

Cumming, H. & Rücker, C., 30.09.2017, In: ACS Omega. 2, 9, p. 6244-6249 6 p.

Research output: Journal contributions › Journal articles › Research › peer-review

DOI

https://doi.org/10.1016/S0040-4039(01)81435-0
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Anionic 1,4 O→C silyl rearrangements

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