Efficient Total Synthesis of Marine Alkaloid (-)-NakadomarinA

Z's top: For the total synthesis of the marine alkaloid (-)-nakadomarinA, (-)-camphorsulfonic acid assisted, Z-selective, olefin RCM of a monoamine (less polar) rather than a diamine (more polar) was found to be highly practical for constructing the Fring. The ABCD-tetracyclic core was assemble...

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Veröffentlicht in:Chemistry : a European journal 2011-11, Vol.17 (45), p.12569-12572
Hauptverfasser: Cheng, Bin, Wu, Fufang, Yang, Xiaobao, Zhou, Yuedong, Wan, Xiaolong, Zhai, Hongbin
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container_end_page 12572
container_issue 45
container_start_page 12569
container_title Chemistry : a European journal
container_volume 17
creator Cheng, Bin
Wu, Fufang
Yang, Xiaobao
Zhou, Yuedong
Wan, Xiaolong
Zhai, Hongbin
description Z's top: For the total synthesis of the marine alkaloid (-)-nakadomarinA, (-)-camphorsulfonic acid assisted, Z-selective, olefin RCM of a monoamine (less polar) rather than a diamine (more polar) was found to be highly practical for constructing the Fring. The ABCD-tetracyclic core was assembled through a novel efficacious PtCl sub(2)-promoted cascade reaction sequence (see scheme).
doi_str_mv 10.1002/chem.201102101
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source Wiley Online Library - AutoHoldings Journals
subjects Alkaloids
Chemistry
Construction
Diamines
Effectiveness
Marine
Olefins
RCM
Synthesis
title Efficient Total Synthesis of Marine Alkaloid (-)-NakadomarinA
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