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A Straightforward Approach to the Synthesis of Disubstituted Cyclopentenones
Author(s) -
Roldão Mariane V.,
SouzaFilho Luis Gustavo,
Almeida Wanda P.,
Coelho Fernando
Publication year - 2020
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201901850
Subject(s) - chemistry , adduct , intramolecular force , yield (engineering) , combinatorial chemistry , rhodium , organic chemistry , catalysis , materials science , metallurgy
In this paper we describe an approach for the synthesis of a set of new diversely di‐substituted cyclopentenones using Morita–Baylis–Hillman (MBH) adducts as building blocks. The synthesis was performed with few steps, but the overall yield reached 34 %. A key step of this approach is a rhodium mediated 1,4‐addition reaction on adequately functionalised MBH adducts, which leads to the creation of cinnamate ester derivatives with high E selectivity. These intermediates were used as substrates for an intramolecular Friedel‐Crafts cyclisation reaction to achieve the required 2,3‐substituted cyclopentenones. As far as we know, this is the first report to describe the synthesis of substituted cyclopentenones that directly employ MBH adducts as building blocks.