The dearomative annulation between N-2-pyridylamidine and CO2 toward pyrido[1,2-a]-1,3,5-triazin-4-ones-Reference-Cited by-同舟云学术

The dearomative annulation between N-2-pyridylamidine and CO2 toward pyrido[1,2-a]-1,3,5-triazin-4-ones

Published:2017 Issue:19 Volume:15 Page:4064-4067
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Xia Minfang¹²³⁴⁵,Hu Weiming¹²³⁴⁵,Sun Song¹²³⁴⁵,Yu Jin-Tao¹²³⁴⁵^ORCID,Cheng Jiang¹²³⁴⁵^ORCID

Affiliation:

1. School of Petrochemical Engineering

2. Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology

3. Jiangsu Province Key Laboratory of Fine Petrochemical Engineering

4. Changzhou University

5. Changzhou

Abstract

A base-promoted dearomative annulation between N-2-pyridylamidine and an atmospheric pressure of CO₂ was developed, affording a series of pyrido[1,2-a]-1,3,5-triazin-4-ones in moderate to excellent yields.

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/C7OB00777A

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