A One-Pot Synthesis of Substituted Pyrrolo[2,1-<i>a</i>]isoquinolines via an Oxidation/Annulation Sequence of 2-(3,4-Dihydroisoquinolin-2(1<i>H</i>)-yl)malononitriles

A highly effective oxidation/annulation reaction between 2-isocyanoacetates and 2-(3,4-dihydroisoquinolin-2(1<i>H</i>)-yl)malononitriles has been successfully developed to give substituted pyrrolo[2,1-<i>a</i>]isoquinoline derivatives with moderate to good yields in a one-pot manner.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-05-15
DOI
https://doi.org/10.1021/acs.joc.5c00639
Citations
2
Primary Topic
Synthesis and Characterization of Pyrroles
Type
article
Field-Weighted Citation Impact
1.87

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article

A One-Pot Synthesis of Substituted Pyrrolo[2,1-a]isoquinolines via an Oxidation/Annulation Sequence of 2-(3,4-Dihydroisoquinolin-2(1H)-yl)malononitriles

Shao‐Hua Wang, Feng Qiu, Wen Bao, K.‐C. HOU et al.
2 citations
The Journal of Organic Chemistry
Synthesis and Characterization of Pyrroles
1.87
article

A One-Pot Synthesis of Substituted Pyrrolo[2,1-a]isoquinolines via an Oxidation/Annulation Sequence of 2-(3,4-Dihydroisoquinolin-2(1H)-yl)malononitriles

Shao‐Hua Wang, Feng Qiu, Wen Bao, K.‐C. HOU, Bang‐Hong Zhang, Ye Zhang, Geoffrey Liu, Runze Li, Dao‐Yong Zhu, Zi-Qin Wei
article en
2 citations

Abstract

A highly effective oxidation/annulation reaction between 2-isocyanoacetates and 2-(3,4-dihydroisoquinolin-2(1<i>H</i>)-yl)malononitriles has been successfully developed to give substituted pyrrolo[2,1-<i>a</i>]isoquinoline derivatives with moderate to good yields in a one-pot manner.

The Journal of Organic ChemistryVol. 90(21)
Lanzhou University (CN)
National Natural Science Foundation of China, Lanzhou Science and Technology Bureau, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities, Science and Technology Program of Gansu Province
Openalex Percentile: Top 16%
Synthesis and Characterization of Pyrroles
1.87
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