'Extension of Ring Closing Metathesis Methodology to the Synthesis of Carbocyclic Methyl and Silyl Enol Ethers'

VK Aggarwal; AM Daly

doi:10.1039/b208445g

'Extension of Ring Closing Metathesis Methodology to the Synthesis of Carbocyclic Methyl and Silyl Enol Ethers'

VK Aggarwal^*, AM Daly

^*Corresponding author for this work

School of Chemistry

Research output: Contribution to journal › Article (Academic Journal) › peer-review

33 Citations (Scopus)

Abstract

Carbocyclic methyl and silyl enol ethers (TBDMS is optimum) can be synthesised regiospecifically by ring closing metathesis using the 'second generation' Grubbs ruthenium carbene catalyst in combination with molecular sieves.

Translated title of the contribution	'Extension of Ring Closing Metathesis Methodology to the Synthesis of Carbocyclic Methyl and Silyl Enol Ethers'
Original language	English
Pages (from-to)	2490-2491
Number of pages	2
Journal	Chemical Communications
Issue number	21
DOIs	https://doi.org/10.1039/b208445g
Publication status	Published - 2002

Keywords

OLEFIN METATHESIS
POLYCYCLIC ETHERS
CATALYST
CONVERGENT
ROUTE

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@article{581acda6a6914e6cbee3164fd73b2eba,

title = "'Extension of Ring Closing Metathesis Methodology to the Synthesis of Carbocyclic Methyl and Silyl Enol Ethers'",

abstract = "Carbocyclic methyl and silyl enol ethers (TBDMS is optimum) can be synthesised regiospecifically by ring closing metathesis using the 'second generation' Grubbs ruthenium carbene catalyst in combination with molecular sieves.",

keywords = "OLEFIN METATHESIS, POLYCYCLIC ETHERS, CATALYST, CONVERGENT, ROUTE",

author = "VK Aggarwal and AM Daly",

year = "2002",

doi = "10.1039/b208445g",

language = "English",

pages = "2490--2491",

journal = "Chemical Communications",

issn = "1364-548X",

publisher = "Royal Society of Chemistry",

number = "21",

}

TY - JOUR

T1 - 'Extension of Ring Closing Metathesis Methodology to the Synthesis of Carbocyclic Methyl and Silyl Enol Ethers'

AU - Aggarwal, VK

AU - Daly, AM

PY - 2002

Y1 - 2002

N2 - Carbocyclic methyl and silyl enol ethers (TBDMS is optimum) can be synthesised regiospecifically by ring closing metathesis using the 'second generation' Grubbs ruthenium carbene catalyst in combination with molecular sieves.

AB - Carbocyclic methyl and silyl enol ethers (TBDMS is optimum) can be synthesised regiospecifically by ring closing metathesis using the 'second generation' Grubbs ruthenium carbene catalyst in combination with molecular sieves.

KW - OLEFIN METATHESIS

KW - POLYCYCLIC ETHERS

KW - CATALYST

KW - CONVERGENT

KW - ROUTE

U2 - 10.1039/b208445g

DO - 10.1039/b208445g

M3 - Article (Academic Journal)

SN - 1364-548X

SP - 2490

EP - 2491

JO - Chemical Communications

JF - Chemical Communications

IS - 21

ER -

'Extension of Ring Closing Metathesis Methodology to the Synthesis of Carbocyclic Methyl and Silyl Enol Ethers'

Abstract

Keywords

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