Tandem Insertion–Cyclization Reaction of Isocyanides in the Synthesis of 1,4-Diaryl-1H-imidazoles: Presence of N-Arylformimidate Intermediate-Reference-Cited by-同舟云学术

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Tandem Insertion–Cyclization Reaction of Isocyanides in the Synthesis of 1,4-Diaryl-1H-imidazoles: Presence of N-Arylformimidate Intermediate

Published:2014-09-18 Issue:19 Volume:79 Page:9231-9245
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Pooi Benjamin¹,Lee Jeongbin¹,Choi Kyujin¹,Hirao Hajime²,Hong Soon Hyeok¹

Affiliation:

1. Department of Chemistry, College of Natural Sciences, Seoul National University, Seoul 151-747, Republic of Korea

2. Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, 637371 Singapore

Funder

National Research Foundation of Korea

Nanyang Technological University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo501652w

Reference119 articles.

1. Ni(II)·Xaa-Xaa-His Metallopeptide−DNA/RNA Interactions

2. Structural and Functional Aspects of Metal Sites in Biology

3. Crystal structure of bovine Cu,Zn superoxide dismutase at 3 A resolution: chain tracing and metal ligands.

4. Vascular Disrupting Activity of Tubulin-Binding 1,5-Diaryl-1H-imidazoles

5. Gesashidine A, a β-Carboline Alkaloid with an Imidazole Ring from a Thorectidae Sponge

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