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01311 am a22002413u 4500 |
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99513 |
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|a dc
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|a Sparling, Brian A.
|e author
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|a Massachusetts Institute of Technology. Department of Chemistry
|e contributor
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|a Sparling, Brian A.
|e contributor
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|a Simpson, Graham L.
|e contributor
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|a Jamison, Timothy F.
|e contributor
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|a Simpson, Graham L.
|e author
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|a Jamison, Timothy F.
|e author
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|a Strategic use of nickel(0)-catalyzed enyne-epoxide reductive coupling toward the synthesis of (−)-cyatha-3,12-diene
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| 260 |
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|b Elsevier,
|c 2015-10-29T17:49:40Z.
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| 856 |
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|z Get fulltext
|u http://hdl.handle.net/1721.1/99513
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|a Various situations are explored in which the nickel(0)-catalyzed enyne-epoxide reductive coupling was utilized to access key intermediates toward the total synthesis of (−)-cyatha-3,12-diene (1). Enantioenriched 3,5-dien-1-ols with a variety of functionality were obtained in a straightforward manner from easily accessible 1,3-enynes and terminal epoxides.
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|a National Institute of General Medical Sciences (U.S.) (GM-063755)
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|a Massachusetts Institute of Technology. Undergraduate Research Opportunities Program
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|a en_US
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|a Article
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|t Tetrahedron
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