Highly regioselective intramolecular biaryl coupling reaction of a phenyl benzoate derivative for the synthesis of graphislactone g

Hitoshi Abe; Takuya Matsukihira; Tomoko Fukumoto; Yoshikazu Horino; Yasuo Takeuchi; Takashi Harayama

doi:10.3987/COM-11-S(P)34

Highly regioselective intramolecular biaryl coupling reaction of a phenyl benzoate derivative for the synthesis of graphislactone g

Hitoshi Abe^*, Takuya Matsukihira, Tomoko Fukumoto, Yoshikazu Horino, Yasuo Takeuchi, Takashi Harayama

^*Corresponding author for this work

Applied Chemistry

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

8 Scopus citations

Abstract

The 6H-dibenzo[b,d]pyran-6-one type natural product graphislactone G was synthesized using a palladium-mediated aryl-aryl coupling reaction of the phenyl benzoate derivative. The regioselectivity in the coupling step was also investigated.

Original language	English
Pages (from-to)	323-326
Number of pages	4
Journal	Heterocycles
Volume	84
Issue number	1
DOIs	https://doi.org/10.3987/COM-11-S(P)34
State	Published - 2011/12/22

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

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title = "Highly regioselective intramolecular biaryl coupling reaction of a phenyl benzoate derivative for the synthesis of graphislactone g",

abstract = "The 6H-dibenzo[b,d]pyran-6-one type natural product graphislactone G was synthesized using a palladium-mediated aryl-aryl coupling reaction of the phenyl benzoate derivative. The regioselectivity in the coupling step was also investigated.",

author = "Hitoshi Abe and Takuya Matsukihira and Tomoko Fukumoto and Yoshikazu Horino and Yasuo Takeuchi and Takashi Harayama",

year = "2011",

month = dec,

day = "22",

doi = "10.3987/COM-11-S(P)34",

language = "英語",

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publisher = "Japan Institute of Heterocyclic Chemistry",

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T1 - Highly regioselective intramolecular biaryl coupling reaction of a phenyl benzoate derivative for the synthesis of graphislactone g

AU - Abe, Hitoshi

AU - Matsukihira, Takuya

AU - Fukumoto, Tomoko

AU - Horino, Yoshikazu

AU - Takeuchi, Yasuo

AU - Harayama, Takashi

PY - 2011/12/22

Y1 - 2011/12/22

N2 - The 6H-dibenzo[b,d]pyran-6-one type natural product graphislactone G was synthesized using a palladium-mediated aryl-aryl coupling reaction of the phenyl benzoate derivative. The regioselectivity in the coupling step was also investigated.

AB - The 6H-dibenzo[b,d]pyran-6-one type natural product graphislactone G was synthesized using a palladium-mediated aryl-aryl coupling reaction of the phenyl benzoate derivative. The regioselectivity in the coupling step was also investigated.

UR - http://www.scopus.com/inward/record.url?scp=84855941163&partnerID=8YFLogxK

U2 - 10.3987/COM-11-S(P)34

DO - 10.3987/COM-11-S(P)34

M3 - 学術論文

AN - SCOPUS:84855941163

SN - 0385-5414

VL - 84

SP - 323

EP - 326

JO - Heterocycles

JF - Heterocycles

IS - 1

ER -

Highly regioselective intramolecular biaryl coupling reaction of a phenyl benzoate derivative for the synthesis of graphislactone g

Abstract

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