Synthesis of a tetracyclic aminobenzimidazole derivative via tandem cyclization of triphenylguanidine

Yuki Akamatsu; Shinichiro Kamino; Daisuke Sawada

doi:10.3987/COM-18-S(F)61

Synthesis of a tetracyclic aminobenzimidazole derivative via tandem cyclization of triphenylguanidine

Yuki Akamatsu, Shinichiro Kamino, Daisuke Sawada

Research output: Contribution to journal › Article

Abstract

We developed a new reaction for the one-pot synthesis of a fused cyclic compound from triphenylguanidine, which was thought to be tandem cyclization, with a moderate yield. In this reaction, conditions such as the metal reagent, oxidant, solvent, and ligand affected whether single or tandem cyclization was preferred.

Original language	English
Pages (from-to)	815-819
Number of pages	5
Journal	Heterocycles
DOIs	https://doi.org/10.3987/COM-18-S(F)61
Publication status	Published - Jan 1 2019

Fingerprint

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

Cite this

Akamatsu, Y., Kamino, S., & Sawada, D. (2019). Synthesis of a tetracyclic aminobenzimidazole derivative via tandem cyclization of triphenylguanidine. Heterocycles, 815-819. https://doi.org/10.3987/COM-18-S(F)61

@article{7d7b258f8dfa4b178ef6cdfdf8a44195,

title = "Synthesis of a tetracyclic aminobenzimidazole derivative via tandem cyclization of triphenylguanidine",

abstract = "We developed a new reaction for the one-pot synthesis of a fused cyclic compound from triphenylguanidine, which was thought to be tandem cyclization, with a moderate yield. In this reaction, conditions such as the metal reagent, oxidant, solvent, and ligand affected whether single or tandem cyclization was preferred.",

author = "Yuki Akamatsu and Shinichiro Kamino and Daisuke Sawada",

year = "2019",

month = jan

day = "1",

doi = "10.3987/COM-18-S(F)61",

language = "English",

pages = "815--819",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

}

TY - JOUR

T1 - Synthesis of a tetracyclic aminobenzimidazole derivative via tandem cyclization of triphenylguanidine

AU - Akamatsu, Yuki

AU - Kamino, Shinichiro

AU - Sawada, Daisuke

PY - 2019/1/1

Y1 - 2019/1/1

N2 - We developed a new reaction for the one-pot synthesis of a fused cyclic compound from triphenylguanidine, which was thought to be tandem cyclization, with a moderate yield. In this reaction, conditions such as the metal reagent, oxidant, solvent, and ligand affected whether single or tandem cyclization was preferred.

AB - We developed a new reaction for the one-pot synthesis of a fused cyclic compound from triphenylguanidine, which was thought to be tandem cyclization, with a moderate yield. In this reaction, conditions such as the metal reagent, oxidant, solvent, and ligand affected whether single or tandem cyclization was preferred.

UR - http://www.scopus.com/inward/record.url?scp=85069684105&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85069684105&partnerID=8YFLogxK

U2 - 10.3987/COM-18-S(F)61

DO - 10.3987/COM-18-S(F)61

M3 - Article

AN - SCOPUS:85069684105

SP - 815

EP - 819

JO - Heterocycles

JF - Heterocycles

SN - 0385-5414

ER -

Access to Document

10.3987/COM-18-S(F)61