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Synlett 2020; 31(13): 1231-1236
DOI: 10.1055/s-0040-1707858
DOI: 10.1055/s-0040-1707858
synpacts
New Organic Dyes from Phthalonitrile via Interesting Nucleophilic Reactions
Funding was provided by the National Natural Science Foundation of China (Grant Nos. 21631006, 21771100 and 21601060) and the Natural Science Foundation of Jiangsu Province (Grant No. BK20170016).Further Information
Publication History
Received: 21 April 2020
Accepted after revision: 07 May 2020
Publication Date:
03 June 2020 (online)
Abstract
Phthalonitrile (PN) is regarded mostly as an important precursor for phthalocyanine (Pc). However, the presence of two ortho triple bonds also endow PN with significant potential to form novel conjugated systems. Based on several unexpected nucleophilic reactions, our group has discovered novel applications of PN for the synthesis of asymmetric benzo-fused aza-BOIDPYs and new fused-ring phthalorubines (Pr). This Synpacts highlights our recent advances in this field.
1 Introduction
2 Benzo-Fused Aza-BODIPYs
3 Phthalorubines
4 Conclusion
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