Application of β-(2-Chloroaroyl) Thioacetanilides in Synthesis: An Unusual and Highly Efficient Access to Thiochromeno[2,3-b]pyridine Derivatives-Reference-Cited by-同舟云学术

Application of β-(2-Chloroaroyl) Thioacetanilides in Synthesis: An Unusual and Highly Efficient Access to Thiochromeno[2,3-b]pyridine Derivatives

Published:2008-01-26 Issue:5 Volume:73 Page:1852-1863
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wen Li-Rong¹,Sun Ji-Hui¹,Li Ming¹,Sun En-Tao¹,Zhang Shu-Sheng¹

Affiliation:

1. Key Laboratory of Eco-Chemical Engineering, Ministry of Education, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo7024702

Reference53 articles.

1. Exploiting the Dual Reactivity of o-Isocyanobenzamide: Three-Component Synthesis of 4-Imino-4H-3,1-benzoxazines

2. Domino Reaction of 3-(2-Formylphenoxy)propenoates and Amines: A Novel Synthesis of 1,4-Dihydropyridines from Salicaldehydes, Ethyl Propiolate, and Amines

3. Chemo-differentiating MCRs based on α-ketoesters and terminal alkynoates. A homoaldol-based ABB′ system

4. Maximizing Synthetic Efficiency: Multi-Component Transformations Lead the Way

5. Domino Reactions in Organic Synthesis

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