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Synthesis of bicyclo[4.2.0]octan-2-ol, a substructure of solanoeclepin A

A sesterterpenoid solanoeclepin A (1) has a unique structure including a bicyclo[4.2.0]octane substructure, for which a new synthetic methodology is explored particularly to cyclize functionalized cyclobutane rings. An optically active ( R)-carvone and a racemic cyclohexenone were each converted int...

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Published in:Tetrahedron letters 2011-04, Vol.52 (16), p.1847-1850
Main Authors: Isobe, Minoru, Niyomchon, Supaporn, Cheng, Chia-Yi, Hasakunpaisarn, Anuch
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Language:English
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description A sesterterpenoid solanoeclepin A (1) has a unique structure including a bicyclo[4.2.0]octane substructure, for which a new synthetic methodology is explored particularly to cyclize functionalized cyclobutane rings. An optically active ( R)-carvone and a racemic cyclohexenone were each converted into the respective epoxyvinylsulfones, and then subjected to the heteroatom-directed conjugate addition (HADCA) by a lithium acetylide nucleophile. The intermediate carbanions from HADCA were used for the following epoxide opening reaction yielding the four-membered carbocyclic products.
doi_str_mv 10.1016/j.tetlet.2011.01.152
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ispartof Tetrahedron letters, 2011-04, Vol.52 (16), p.1847-1850
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1873-3581
language eng
recordid cdi_proquest_miscellaneous_1744676633
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subjects Alicyclic compounds
Alicyclic compounds, terpenoids, prostaglandins, steroids
Chemistry
Conjugates
Cyclobutane
Exact sciences and technology
Heterocyclic compounds
Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives
Lithium
Nucleophiles
Optical activity
Organic chemistry
Preparations and properties
Substructures
Synthesis (chemistry)
Terpenoids
Tetrahedrons
title Synthesis of bicyclo[4.2.0]octan-2-ol, a substructure of solanoeclepin A
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