Extremely facile formation and high reactivity of new thioacylsilanes containing the ferrocene moiety

Bianca F. Bonini; Mauro Comes-Franchini; Mariafrancesca Fochi; Germana Mazzanti; Alfredo Ricci; Greta Varchi

doi:10.1016/S0040-4039(99)01218-6

Extremely facile formation and high reactivity of new thioacylsilanes containing the ferrocene moiety

Bianca F. Bonini, Mauro Comes-Franchini, Mariafrancesca Fochi, Germana Mazzanti, Alfredo Ricci, Greta Varchi

Houston Methodist

Research output: Contribution to journal › Article › peer-review

33 Scopus citations

Abstract

Thioacylsilanes containing the ferrocene moiety, easily prepared from the corresponding acylsilanes with Lawesson's reagent at room temperature, can be transformed into vinyl silanes, sulfur heterocycles and sulfines.

Original language	English (US)
Pages (from-to)	6473-6476
Number of pages	4
Journal	Tetrahedron Letters
Volume	40
Issue number	35
DOIs	https://doi.org/10.1016/S0040-4039(99)01218-6
State	Published - Aug 27 1999

Keywords

Acylsilanes
Ferrocene derivatives
Thioacylsilanes
Vinylsilanes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(99)01218-6

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title = "Extremely facile formation and high reactivity of new thioacylsilanes containing the ferrocene moiety",

abstract = "Thioacylsilanes containing the ferrocene moiety, easily prepared from the corresponding acylsilanes with Lawesson's reagent at room temperature, can be transformed into vinyl silanes, sulfur heterocycles and sulfines.",

keywords = "Acylsilanes, Ferrocene derivatives, Thioacylsilanes, Vinylsilanes",

author = "Bonini, \{Bianca F.\} and Mauro Comes-Franchini and Mariafrancesca Fochi and Germana Mazzanti and Alfredo Ricci and Greta Varchi",

note = "Funding Information: This work has been supported by University of Bologna (Funds for Selected Research Topics, A.A. 1995-1997) and by the National Project Stereoselezione in Sintesi Organica, Metodologie ed Applicazioni. Copyright: Copyright 2007 Elsevier B.V., All rights reserved.",

year = "1999",

month = aug,

day = "27",

doi = "10.1016/S0040-4039(99)01218-6",

language = "English (US)",

volume = "40",

pages = "6473--6476",

journal = "Tetrahedron Letters",

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T1 - Extremely facile formation and high reactivity of new thioacylsilanes containing the ferrocene moiety

AU - Bonini, Bianca F.

AU - Comes-Franchini, Mauro

AU - Fochi, Mariafrancesca

AU - Mazzanti, Germana

AU - Ricci, Alfredo

AU - Varchi, Greta

N1 - Funding Information: This work has been supported by University of Bologna (Funds for Selected Research Topics, A.A. 1995-1997) and by the National Project Stereoselezione in Sintesi Organica, Metodologie ed Applicazioni. Copyright: Copyright 2007 Elsevier B.V., All rights reserved.

PY - 1999/8/27

Y1 - 1999/8/27

N2 - Thioacylsilanes containing the ferrocene moiety, easily prepared from the corresponding acylsilanes with Lawesson's reagent at room temperature, can be transformed into vinyl silanes, sulfur heterocycles and sulfines.

AB - Thioacylsilanes containing the ferrocene moiety, easily prepared from the corresponding acylsilanes with Lawesson's reagent at room temperature, can be transformed into vinyl silanes, sulfur heterocycles and sulfines.

KW - Acylsilanes

KW - Ferrocene derivatives

KW - Thioacylsilanes

KW - Vinylsilanes

UR - https://www.scopus.com/pages/publications/0033609874

UR - https://www.scopus.com/inward/citedby.url?scp=0033609874&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(99)01218-6

DO - 10.1016/S0040-4039(99)01218-6

M3 - Article

AN - SCOPUS:0033609874

SN - 0040-4039

VL - 40

SP - 6473

EP - 6476

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 35

ER -

Extremely facile formation and high reactivity of new thioacylsilanes containing the ferrocene moiety

Abstract

Keywords

ASJC Scopus subject areas

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