A novel synthesis of acylsilanes

Masahisa Nakada; Sei ichi Nakamura; Susumu Kobayashi; Masaji Ohno

doi:10.1016/S0040-4039(00)93499-3

A novel synthesis of acylsilanes

Masahisa Nakada, Sei ichi Nakamura, Susumu Kobayashi, Masaji Ohno

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

23 Citations (Scopus)

Abstract

A mild and general preparative method for acylsilane is presented. This novel method can be applied without any difficulty to α-chiral, α-alkoxy and multifunctionalized compounds.

Original language	English
Pages (from-to)	4929-4932
Number of pages	4
Journal	Tetrahedron Letters
Volume	32
Issue number	37
DOIs	https://doi.org/10.1016/S0040-4039(00)93499-3
Publication status	Published - 1991 Sep 9
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(00)93499-3

Fingerprint Dive into the research topics of 'A novel synthesis of acylsilanes'. Together they form a unique fingerprint.

Cite this

@article{8f6e51e15e424b799731d77c537a09d5,

title = "A novel synthesis of acylsilanes",

abstract = "A mild and general preparative method for acylsilane is presented. This novel method can be applied without any difficulty to α-chiral, α-alkoxy and multifunctionalized compounds.",

author = "Masahisa Nakada and Nakamura, {Sei ichi} and Susumu Kobayashi and Masaji Ohno",

year = "1991",

month = sep,

day = "9",

doi = "10.1016/S0040-4039(00)93499-3",

language = "English",

volume = "32",

pages = "4929--4932",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "37",

}

TY - JOUR

T1 - A novel synthesis of acylsilanes

AU - Nakada, Masahisa

AU - Nakamura, Sei ichi

AU - Kobayashi, Susumu

AU - Ohno, Masaji

PY - 1991/9/9

Y1 - 1991/9/9

N2 - A mild and general preparative method for acylsilane is presented. This novel method can be applied without any difficulty to α-chiral, α-alkoxy and multifunctionalized compounds.

AB - A mild and general preparative method for acylsilane is presented. This novel method can be applied without any difficulty to α-chiral, α-alkoxy and multifunctionalized compounds.

UR - http://www.scopus.com/inward/record.url?scp=0025774153&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0025774153&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)93499-3

DO - 10.1016/S0040-4039(00)93499-3

M3 - Article

AN - SCOPUS:0025774153

VL - 32

SP - 4929

EP - 4932

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 37

ER -