Synthetic study of the c'd'e' ring system of maitotoxin via furan based strategy

Yuta Watanabe; Kohei Torikai; Yoko Yasuno; Tohru Oishi

doi:10.3987/COM-21-14545

Synthetic study of the c'd'e' ring system of maitotoxin via furan based strategy

Yuta Watanabe
, Kohei Torikai
, Yoko Yasuno
, Tohru Oishi

Organic and Biological Chemistry

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

3 Citations (Scopus)

Abstract

Synthetic study of the C'D'E' ring system of maitotoxin was examined via Suzuki-Miyaura coupling of an exo-iodoolefin and a furanylborane derivative, followed by Sharpless asymmetric dihydroxylation, Achmatowicz reaction, borylation/oxidation, and reductive etherification.

Original language	English
Pages (from-to)	2313-2318
Number of pages	6
Journal	Heterocycles
Volume	102
Issue number	12
DOIs	https://doi.org/10.3987/COM-21-14545
Publication status	Published - 2021

All Science Journal Classification (ASJC) codes

Analytical Chemistry
Pharmacology
Organic Chemistry

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10.3987/COM-21-14545

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title = "Synthetic study of the c'd'e' ring system of maitotoxin via furan based strategy",

abstract = "Synthetic study of the C'D'E' ring system of maitotoxin was examined via Suzuki-Miyaura coupling of an exo-iodoolefin and a furanylborane derivative, followed by Sharpless asymmetric dihydroxylation, Achmatowicz reaction, borylation/oxidation, and reductive etherification.",

author = "Yuta Watanabe and Kohei Torikai and Yoko Yasuno and Tohru Oishi",

year = "2021",

doi = "10.3987/COM-21-14545",

language = "English",

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publisher = "Japan Institute of Heterocyclic Chemistry",

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T1 - Synthetic study of the c'd'e' ring system of maitotoxin via furan based strategy

AU - Watanabe, Yuta

AU - Torikai, Kohei

AU - Yasuno, Yoko

AU - Oishi, Tohru

PY - 2021

Y1 - 2021

N2 - Synthetic study of the C'D'E' ring system of maitotoxin was examined via Suzuki-Miyaura coupling of an exo-iodoolefin and a furanylborane derivative, followed by Sharpless asymmetric dihydroxylation, Achmatowicz reaction, borylation/oxidation, and reductive etherification.

AB - Synthetic study of the C'D'E' ring system of maitotoxin was examined via Suzuki-Miyaura coupling of an exo-iodoolefin and a furanylborane derivative, followed by Sharpless asymmetric dihydroxylation, Achmatowicz reaction, borylation/oxidation, and reductive etherification.

UR - https://www.scopus.com/pages/publications/85120944317

UR - https://www.scopus.com/pages/publications/85120944317#tab=citedBy

U2 - 10.3987/COM-21-14545

DO - 10.3987/COM-21-14545

M3 - Article

AN - SCOPUS:85120944317

SN - 0385-5414

VL - 102

SP - 2313

EP - 2318

JO - Heterocycles

JF - Heterocycles

IS - 12

ER -

Synthetic study of the c'd'e' ring system of maitotoxin via furan based strategy

Abstract

All Science Journal Classification (ASJC) codes

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