Tetrahedron letters2022,Vol.905.DOI:10.1016/j.tetlet.2021.153608

Synthesis of the eight-membered carbocycle of brachialactone by intramolecular Mizoroki-Heck reaction

Nakazaki A. Nishikawa T. Hirata Y.
Tetrahedron letters2022,Vol.905.DOI:10.1016/j.tetlet.2021.153608

Synthesis of the eight-membered carbocycle of brachialactone by intramolecular Mizoroki-Heck reaction

Nakazaki A. 1Nishikawa T. 1Hirata Y.1
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作者信息

  • 1. Graduate School of Bioagricultural Sciences Nagoya University
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Abstract

? 2021 Elsevier LtdA synthesis of the BC ring moiety of brachialactone, a fusicoccane-type diterpene isolated from the tropical forage grass Brachiaria humidicola and found to inhibit nitrification by soil microbes, is described. Several precursors including the C ring were synthesized from a known chiral cyclopentane, and then subjected to the conditions for the Mizoroki-Heck reaction. Substrates incorporating vinyl (R = H) or enone (R = COCH3) moieties and incorporating an S configuration at C-2 successfully underwent intramolecular Mizoroki-Heck reaction, giving the BC ring structure of brachialactone.

Key words

Brachialactone/Fusicoccane/Intramolecular Mizoroki-Heck reaction/Natural product synthesis

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出版年

2022
Tetrahedron letters

Tetrahedron letters

CCR
ISSN:0040-4039
参考文献量62
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