Synthesis of Fasicularin

Atsushi Kaga; Ya Lin Tnay; Shunsuke Chiba

doi:10.1021/acs.orglett.6b01669

Synthesis of Fasicularin

Atsushi Kaga, Ya Lin Tnay, Shunsuke Chiba^*

^*Corresponding author for this work

Nanyang Technological University

Research output: Contribution to journal › Article › peer-review

10 Citations (Scopus)

Abstract

The synthesis of a tricyclic marine alkaloid, fasicularin, was accomplished. Stereoselective synthesis of the aza-spirocyclic BC-ring precursor and ensuing construction of the A-ring with stereocontrolled installation of the C2 hexyl group feature prominently in the synthesis.

Original language	English
Pages (from-to)	3506-3508
Number of pages	3
Journal	Organic Letters
Volume	18
Issue number	14
DOIs	https://doi.org/10.1021/acs.orglett.6b01669
Publication status	Published - Jul 15 2016
Externally published	Yes

Bibliographical note

Publisher Copyright:
© 2016 American Chemical Society.

ASJC Scopus Subject Areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1021/acs.orglett.6b01669

Cite this

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title = "Synthesis of Fasicularin",

abstract = "The synthesis of a tricyclic marine alkaloid, fasicularin, was accomplished. Stereoselective synthesis of the aza-spirocyclic BC-ring precursor and ensuing construction of the A-ring with stereocontrolled installation of the C2 hexyl group feature prominently in the synthesis.",

author = "Atsushi Kaga and Tnay, \{Ya Lin\} and Shunsuke Chiba",

note = "Publisher Copyright: {\textcopyright} 2016 American Chemical Society.",

year = "2016",

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day = "15",

doi = "10.1021/acs.orglett.6b01669",

language = "English",

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journal = "Organic Letters",

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AU - Tnay, Ya Lin

AU - Chiba, Shunsuke

PY - 2016/7/15

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N2 - The synthesis of a tricyclic marine alkaloid, fasicularin, was accomplished. Stereoselective synthesis of the aza-spirocyclic BC-ring precursor and ensuing construction of the A-ring with stereocontrolled installation of the C2 hexyl group feature prominently in the synthesis.

AB - The synthesis of a tricyclic marine alkaloid, fasicularin, was accomplished. Stereoselective synthesis of the aza-spirocyclic BC-ring precursor and ensuing construction of the A-ring with stereocontrolled installation of the C2 hexyl group feature prominently in the synthesis.

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M3 - Article

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JO - Organic Letters

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Synthesis of Fasicularin

Abstract

Bibliographical note

ASJC Scopus Subject Areas

UN SDGs

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