Highly Efficient and Diastereoselective Construction of Tricyclic Pyrrolidine‐Fused Benzo[ b ]thiophene 1,1‐dioxide Derivatives via 1,3‐Dipolar [3 + 2] Cycloaddition-Reference-Cited by-同舟云学术

Highly Efficient and Diastereoselective Construction of Tricyclic Pyrrolidine‐Fused Benzo[ b ]thiophene 1,1‐dioxide Derivatives via 1,3‐Dipolar [3 + 2] Cycloaddition

Published:2019-06-18 Issue:8 Volume:56 Page:2274-2280
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J. Heterocyclic Chem.

Author:

Wang Kai‐Kai¹^ORCID,Li Yan‐Li²,Ma Guo‐Yang¹,Yi Meng‐Hao¹,Zhu Bao‐Ku³

Affiliation:

1. College of Chemistry and Chemical EngineeringXinxiang University Xinxiang 453000 People's Republic of China

2. Medical CollegeXinxiang University Xinxiang 453000 People's Republic of China

3. MOE Key Laboratory of Macromolecular Synthesis and FunctionalizationZhejiang University Hangzhou 310058 People's Republic of China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.3591

Reference48 articles.

1. Fused tricyclic pyrrolizinones that exhibit pseudo-irreversible blockade of the NK1 receptor

2. Posttranslational isoprenylation of tryptophan in bacteria

3. Pharmaceuticals that contain polycyclic hydrocarbon scaffolds

4. Synergistic Catalysis for the Asymmetric [3+2] Cycloaddition of Vinyl Aziridines with α,β-Unsaturated Aldehydes

5. N-Heterocyclic-Carbene-Catalyzed Stereoselective Annulations: An Efficient Strategy for the Synthesis of Chromeno[4,3-b]pyrrolidine Derivatives

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