Catalyst‐free 1,6‐Conjugate Addition of S ‐Nucleophiles to para ‐Quinone Methides
Author:
Affiliation:
1. School of Pharmaceutical Sciences College of Chemistry and Chemical Engineering Liaocheng University Liaocheng 252000 Shandong P. R. China
2. The Non-Public Enterprise Service Center of Liaocheng Liaocheng 252000 Shandong P. R. China
Funder
Natural Science Foundation of Shandong Province
National Natural Science Foundation of China
Publisher
Wiley
Subject
Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajoc.202200524
Reference139 articles.
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5. Organic Semiconductors Based on [1]Benzothieno[3,2-b][1]benzothiophene Substructure
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Phosphine‐Catalyzed 1,6‐Addition and Tandem Addition/Self‐Aldol Condensation Reactions of Para‐Quinone Methides with Thiols;European Journal of Organic Chemistry;2024-04-10
2. Synthesis of diarylmethyl thioethersviaa DABCO-catalyzed 1,6-conjugate addition reaction ofp-quinone methides with organosulfur reagents;RSC Advances;2023
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