Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction

Hitoshi Abe; Toshitaka Kawai; Yoshinori Komatsu; Mayu Kamimura; Yasuo Takeuchi; Yoshikazu Horino

doi:10.3987/COM-12-S(N)87

Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction

Hitoshi Abe, Toshitaka Kawai, Yoshinori Komatsu, Mayu Kamimura, Yasuo Takeuchi, Yoshikazu Horino

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

6 Citations (Scopus)

Abstract

Neo-tanshinlactone (1) was synthesized by the intramolecular aryl-aryl coupling reaction of the precursor ester, which was prepared from the corresponding furan carboxylic acid (13) and naphthol (3), using a palladium reagent.

Original language	English
Pages (from-to)	785-789
Number of pages	5
Journal	Heterocycles
Volume	86
Issue number	1
DOIs	https://doi.org/10.3987/COM-12-S(N)87
Publication status	Published - 2012

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

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title = "Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction",

abstract = "Neo-tanshinlactone (1) was synthesized by the intramolecular aryl-aryl coupling reaction of the precursor ester, which was prepared from the corresponding furan carboxylic acid (13) and naphthol (3), using a palladium reagent.",

author = "Hitoshi Abe and Toshitaka Kawai and Yoshinori Komatsu and Mayu Kamimura and Yasuo Takeuchi and Yoshikazu Horino",

year = "2012",

doi = "10.3987/COM-12-S(N)87",

language = "English",

volume = "86",

pages = "785--789",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

number = "1",

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T1 - Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction

AU - Abe, Hitoshi

AU - Kawai, Toshitaka

AU - Komatsu, Yoshinori

AU - Kamimura, Mayu

AU - Takeuchi, Yasuo

AU - Horino, Yoshikazu

PY - 2012

Y1 - 2012

N2 - Neo-tanshinlactone (1) was synthesized by the intramolecular aryl-aryl coupling reaction of the precursor ester, which was prepared from the corresponding furan carboxylic acid (13) and naphthol (3), using a palladium reagent.

AB - Neo-tanshinlactone (1) was synthesized by the intramolecular aryl-aryl coupling reaction of the precursor ester, which was prepared from the corresponding furan carboxylic acid (13) and naphthol (3), using a palladium reagent.

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U2 - 10.3987/COM-12-S(N)87

DO - 10.3987/COM-12-S(N)87

M3 - Article

AN - SCOPUS:84880645113

SN - 0385-5414

VL - 86

SP - 785

EP - 789

JO - Heterocycles

JF - Heterocycles

IS - 1

ER -

Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction

Abstract

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