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An isomerization-ring-closing metathesis strategy for the synthesis of substituted benzofurans

Tetrahedron, Volume 61, No. 32, Year 2005

Twelve substituted benzofurans were synthesized from their corresponding substituted 1-allyl-2-allyloxybenzenes using ruthenium-mediated C- and O-allyl isomerization followed by ring-closing metathesis. © 2005 Elsevier Ltd. All rights reserved.

van Otterlo, Willem A. L.
1. South Africa, Johannesburg University of the Witwatersrand
Morgans, Garreth L.
1. South Africa, Johannesburg University of the Witwatersrand
Madeley, Lee G.
1. South Africa, Johannesburg University of the Witwatersrand
Kuzvidza, Samuel
1. South Africa, Johannesburg University of the Witwatersrand
Mnyakeni-Moleele, Simon S.
1. South Africa, Johannesburg University of the Witwatersrand
Thornton, Natalie
1. South Africa, Johannesburg University of the Witwatersrand
de Koning, Charles Bernard D.E.
1. South Africa, Johannesburg University of the Witwatersrand

AFRICAN RESEARCH NEXUS

An isomerization-ring-closing metathesis strategy for the synthesis of substituted benzofurans

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AFRICAN RESEARCH NEXUS

An isomerization-ring-closing metathesis strategy for the synthesis of substituted benzofurans

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African Research Nexus

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