A formal, stereoselective synthesis of the natural tetrahydropyran derivative ophiocerin D
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Other documents of the author: Paños Pérez, Julián; Murga, Juan; Falomir, Eva; Carda, Miguel; Marco, J. Alberto
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comunitat-uji-handle2:10234/7053
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http://dx.doi.org/10.1016/j.tetasy.2010.01.013 |
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Title
A formal, stereoselective synthesis of the natural tetrahydropyran derivative ophiocerin DDate
2010Publisher
ElsevierISSN
9574166Bibliographic citation
Tetrahedron Asymmetry, 21, 4, p. 425-428Type
info:eu-repo/semantics/articleAbstract
A short, formal stereoselective synthesis of the naturally occurring tetrahydropyran derivative ophiocerin D is reported. The four stereocenters of the molecule were created with the aid of two Sharpless asymmetric ... [+]
A short, formal stereoselective synthesis of the naturally occurring tetrahydropyran derivative ophiocerin D is reported. The four stereocenters of the molecule were created with the aid of two Sharpless asymmetric dihydroxylations. © 2010 Elsevier Ltd. All rights reserved. [-]
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