Hypervalent iodine-triggered transformation of homopropargyl sulfonamides into dihalo-2,3-dihydropyrroles-Reference-Cited by-同舟云学术

Hypervalent iodine-triggered transformation of homopropargyl sulfonamides into dihalo-2,3-dihydropyrroles

Published:2017 Issue:4 Volume:15 Page:796-800
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wang Ruijia¹²³⁴⁵,OuYang Yuejun⁶⁷⁵,Xu Chonghui¹²³⁴⁵,Yi Niannian¹²³⁴⁵,Jiang Jun¹²³⁴⁵,Deng Wei¹²³⁴⁵,Zeng Zebing¹²³⁴⁵,Xiang Jiannan¹²³⁴⁵^ORCID

Affiliation:

1. State Key Laboratory of Chemo/Biosensing and Chemometrics

2. College of Chemistry and Chemical Engineering

3. Hunan University

4. Changsha

5. P. R. China

6. Huaihua Key Laboratory of Functional Inorganic & Polymaterial Materials (Huaihua University)

7. Huaihua 418000

Abstract

A novel hypervalent iodine-triggered hydroamination of homopropargyl sulfonamides with copper halides to obtain dihalo-2,3-dihydropyrroles was efficiently developed.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C6OB02536F

Reference59 articles.

1. Pyrrole- and Dihydropyrrole-Fused Neonicotinoids: Design, Synthesis, and Insecticidal Evaluation

2. Synthesis of DNA-Interactive Pyrrolo[2,1-c][1,4]benzodiazepines (PBDs)

3. Pyrrolinone-Based Peptidomimetics.“Let the Enzyme or Receptor be the Judge”

4. Biosynthesis of Sibiromycin, a Potent Antitumor Antibiotic

5. Novel three-component synthesis and antiproliferative properties of diversely functionalized pyrrolines

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