Ring Enlargement Reaction of C,N-Cyclic-N′-acyl Azomethine Imines with Sulfonium Ylide: An Efficient Synthesis of 3-Benzazepine Derivatives-Reference-Cited by-同舟云学术

Ring Enlargement Reaction of C,N-Cyclic-N′-acyl Azomethine Imines with Sulfonium Ylide: An Efficient Synthesis of 3-Benzazepine Derivatives

Published:2014-09-08 Issue:18 Volume:16 Page:4854-4857
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Soeta Takahiro¹,Ohgai Takahiro¹,Sakai Takahiro¹,Fujinami Shuhei¹,Ukaji Yutaka¹

Affiliation:

1. Division of Material Chemistry, Graduate School of Natural Science and Technology, Kanazawa University, Kakuma, Kanazawa 920-1192, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol502347n

Reference63 articles.

1. aVaquero, J. J.; Cuadro, A. M.; Herradón, BInModern Heterocyclic Chemistry;Alvarez-Builla, J., Vaquero, J. J., Barluenga, J., Ed.Willey-VCH:Germany, 2011; pp1865–1988and references cited therein.

2. Design and Synthesis of trans-3-(2-(4-((3-(3-(5-Methyl-1,2,4-oxadiazolyl))- phenyl)carboxamido)cyclohexyl)ethyl)-7-methylsulfonyl-2,3,4,5-tetrahydro- 1H-3-benzazepine (SB-414796): A Potent and Selective Dopamine D3 Receptor Antagonist

3. Ivabradine Hydrochloride

4. Chemistry and biological activity of new 3-benzazepines

5. 6-Hydroxy-3-propyl-2,3,4,5-tetrahydro-1H-3-benzazepine and analogs: new centrally acting 5-HT1a receptor agonists

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