Synthesis of Bicyclo[4.1.0]tetrahydropyridazines by a Sequential [4 + 2] and [1 + 2] Annulation Reaction of Azoalkenes and Crotonate-Derived Sulfur Ylides-Reference-Cited by-同舟云学术

Synthesis of Bicyclo[4.1.0]tetrahydropyridazines by a Sequential [4 + 2] and [1 + 2] Annulation Reaction of Azoalkenes and Crotonate-Derived Sulfur Ylides

Published:2019-09-04 Issue:18 Volume:21 Page:7361-7364
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yin Wenhao¹,Fang Ling²,Wang Zhiyong¹,Gao Fang¹^ORCID,Li Zhefeng¹,Wang Zhiyong¹

Affiliation:

1. School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China

2. College of Environment and Resources, Chongqing Technology and Business University, Chongqing 400067, China

Funder

Ministry of Education of the People's Republic of China

Natural Science Foundation of Chongqing

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02661

Reference63 articles.

1. Synthesis and SAR of 1,4,5,6-tetrahydropyridazines as potent cannabinoid CB1 receptor antagonists

2. Synthesis and evaluation of 1,4,5,6-tetrahydropyridazine derivatives as influenza neuraminidase inhibitors

3. Nonsteroidal progesterone receptor ligands. 1. 3-Aryl-1-benzoyl-1,4,5,6- tetrahydropyridazines.

4. Nonsteroidal Progesterone Receptor Ligands. 2. High-Affinity Ligands with Selectivity for Bone Cell Progesterone Receptors

5. Recent advances in the total synthesis of cyclopropane-containing natural products

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