Total Synthesis of (+)-Azaspiracid-1. An Exhibition of the Intricacies of Complex Molecule Synthesis

The synthesis of the marine neurotoxin azaspiracid-1 has been accomplished. The individual fragments were synthesized by catalytic enantioselective processes: A hetero-Diels−Alder reaction to afford the E- and HI-ring fragments, a carbonyl-ene reaction to furnish the CD-ring fragment, and a Mukaiyam...

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Veröffentlicht in:Journal of the American Chemical Society 2008-12, Vol.130 (48), p.16295-16309
Hauptverfasser: Evans, David A, Kværnø, Lisbet, Dunn, Travis B, Beauchemin, André, Raymer, Brian, Mulder, Jason A, Olhava, Edward J, Juhl, Martin, Kagechika, Katsuji, Favor, David A
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Sprache:eng
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