The synthetic studies of carbazole alkaloids

Hajime Yokoyama; Yuzen Shoji; Takayoshi Kubo; Masahiro Miyazawa; Yoshiro Hirai

doi:10.3987/COM-15-13286

The synthetic studies of carbazole alkaloids

Hajime Yokoyama^*, Yuzen Shoji, Takayoshi Kubo, Masahiro Miyazawa, Yoshiro Hirai

^*Corresponding author for this work

Department of Chemistry

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

2 Scopus citations

Abstract

The carbazole alkaloids have profound biological activities and material properties. We reported that 3, 4-substituted, 3-substituted and 4-substituted carbazoles were regioselectively synthesized from indoline derivatives by means of Diels-Alder reaction in the presence or absence of Pd catalyst and attained the synthesis of natural carbazole alkaloid from 3-substituted carbazole, too.

Original language	English
Pages (from-to)	1752-1762
Number of pages	11
Journal	Heterocycles
Volume	91
Issue number	9
DOIs	https://doi.org/10.3987/COM-15-13286
State	Published - 2015

ASJC Scopus subject areas

Organic Chemistry

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title = "The synthetic studies of carbazole alkaloids",

abstract = "The carbazole alkaloids have profound biological activities and material properties. We reported that 3, 4-substituted, 3-substituted and 4-substituted carbazoles were regioselectively synthesized from indoline derivatives by means of Diels-Alder reaction in the presence or absence of Pd catalyst and attained the synthesis of natural carbazole alkaloid from 3-substituted carbazole, too.",

author = "Hajime Yokoyama and Yuzen Shoji and Takayoshi Kubo and Masahiro Miyazawa and Yoshiro Hirai",

note = "Publisher Copyright: {\textcopyright} 2015 The Japan Institute of Heterocyclic Chemistry.",

year = "2015",

doi = "10.3987/COM-15-13286",

language = "英語",

volume = "91",

pages = "1752--1762",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

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TY - JOUR

T1 - The synthetic studies of carbazole alkaloids

AU - Yokoyama, Hajime

AU - Shoji, Yuzen

AU - Kubo, Takayoshi

AU - Miyazawa, Masahiro

AU - Hirai, Yoshiro

PY - 2015

Y1 - 2015

N2 - The carbazole alkaloids have profound biological activities and material properties. We reported that 3, 4-substituted, 3-substituted and 4-substituted carbazoles were regioselectively synthesized from indoline derivatives by means of Diels-Alder reaction in the presence or absence of Pd catalyst and attained the synthesis of natural carbazole alkaloid from 3-substituted carbazole, too.

AB - The carbazole alkaloids have profound biological activities and material properties. We reported that 3, 4-substituted, 3-substituted and 4-substituted carbazoles were regioselectively synthesized from indoline derivatives by means of Diels-Alder reaction in the presence or absence of Pd catalyst and attained the synthesis of natural carbazole alkaloid from 3-substituted carbazole, too.

UR - http://www.scopus.com/inward/record.url?scp=84949009434&partnerID=8YFLogxK

U2 - 10.3987/COM-15-13286

DO - 10.3987/COM-15-13286

M3 - 学術論文

AN - SCOPUS:84949009434

SN - 0385-5414

VL - 91

SP - 1752

EP - 1762

JO - Heterocycles

JF - Heterocycles

IS - 9

ER -

The synthetic studies of carbazole alkaloids

Abstract

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