Enantioselective Total Syntheses of Marine Natural Products (+)-Cylindricines C, D, E and Their Diastereomers
A seven-step total synthesis of (+)-cylindricine D and epi-cylindricine D is described. The efficiency relies on the highly diastereoselective reductive bis-functionalization of N,O-protected (S)-pyroglutaminol by our recently improved protocol to...
2009 ◽
Vol 74
(6)
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pp. 887-900
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2017 ◽
Vol 15
(22)
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pp. 4842-4850
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2005 ◽
Vol 46
(31)
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pp. 5219-5223
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1985 ◽
Vol 50
(20)
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pp. 3738-3749
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