DBU‐Promoted [3+2] Cyclization/Retro‐Mannich Cascade Reaction of N‐Aminoisoquinolinium and N‐Aminoquinolinium Derivatives with para‐Quinone Methides

Ma, Shaohong; Chen, Mingyang; Yang, Zifeng; Liu, Xiang; Cao, Hua

doi:10.1002/adsc.202400044

Adv Synth Catal

2024

DOI: 10.1002/adsc.202400044

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DBU‐Promoted [3+2] Cyclization/Retro‐Mannich Cascade Reaction of N‐Aminoisoquinolinium and N‐Aminoquinolinium Derivatives with para‐Quinone Methides

Shaohong Ma,

Mingyang Chen,

Zifeng Yang

et al.

Abstract: A DBU‐promoted [3 + 2] cyclization/retro‐Mannich cascade reaction of N‐aminoisoquinolinium and N‐aminoquinolinium derivatives with para‐quinone methides has been established employing a C=C double bond cleavage. A broad range of N‐aminoquinolinium salts, N‐aminoisoquinolinium salts, and para‐quinone methides are well tolerated, providing the corresponding rearrangement products. Moreover, scaled‐up reactions and diverse derivatizations of the products were also investigated and discussed.

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Emerging Trends for the Direct Synthesis of Dithiocarbamates

He,

Zhou,

Liu

2024

Adv Synth Catal

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Dithiocarbamates are common structural motifs in various bioactive compounds, attracting considerable attention due to their wide‐ranging applications in organic synthesis, material science, agrochemicals, and the pharmaceutical industry. Given the significant bioactivity and extensive applications of dithiocarbamates, the continuous pursuit of their efficient and diverse synthetic methods remains critical and urgent. Direct dithiocarbamation reactions can introduce ‐S‐C(S)NR2 group directly into parent molecules, providing shorter, greener, and more practical pathways for the synthesis of organodithiocarbamates. This article offers a comprehensive overview of the latest advancements in direct dithiocarbamation reactions, categorizing them based on the different sources of the ‐S‐C(S)NR2 group, with a particular emphasis on elucidating substrate scope and reaction mechanisms. Additionally, some synthetic limitations and applications of these methods are discussed. This review aims to provide the latest advancements in this field to both general readers and professional practitioners, inspiring innovative ideas for the synthesis of organosulfur compounds.

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Emerging Trends for the Direct Synthesis of Dithiocarbamates

He,

Zhou,

Liu

2024

Adv Synth Catal

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Divergent Assembly of Functionalized Pyrazolo[1,5‐a]pyridine Derivatives via [3+2] Cyclization of N‐Aminopyridinium Salts with Various Unsaturated Hydrocarbons

Liu,

Ma,

Yan

et al. 2024

Chin. J. Chem.

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Comprehensive SummaryTwo reaction modes for metal‐free [3 + 2] cyclization of N‐aminopyridinium derivatives with β‐alkoxyvinyl trifluoromethylketones have been described through selective C—O or C—O/C—C bond cleavage. This strategy can also be extended to the [3 + 2] cyclization of N‐aminopyridinium derivatives with enaminones and bromoalkynes. A broad range of N‐aminopyridinium, N‐aminoquinolinium, and N‐aminoisoquinolinium salts are well tolerated, enabling the divergent synthesis of trifluoroacylated, non‐substituted, acylated, and brominated pyrazolo[1,5‐a]pyridine derivatives (62 examples).

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Recent Advances on the Construction of Functionalized Indolizine and Imidazo[1,2‐a]pyridine Derivatives

Liu,

Fu,

et al. 2024

The Chemical Record

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Indolizines and imidazo[1,2‐a]pyridines are commonly found in natural products, synthetic drugs, and bioactive molecules. These two types of derivatives possess good antibacterial, antiparasitic, anticancer activities, and so on. The functionalization of indolizines and imidazo[1,2‐a]pyridines has always been a hot topic in organic chemistry research and has made significant progress. In recent years, our group has been dedicated to developing diverse synthetic methods for the preparation of such important compounds. 1) We have developed diverse C−H functionalization reactions for efficient modification of the parent indolizines and imidazo[1,2‐a]pyridines. 2) A variety of cycloaddition reactions were established for the construction of indolizine and imidazo[1,2‐a]pyridine derivatives from simple raw materials. 3) We have developed intriguing deconstruction‐functionalization reactions of indolizines, enabling the reorganization of heterocyclic frameworks. This paper outlines our group's latest advancements in constructing structurally diverse indolizine and imidazo[1,2‐a]pyridine derivatives. We hope that this work will offer valuable insights and inspiration for the ongoing research in the field of N‐heterocyclic compounds.

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DBU‐Promoted [3+2] Cyclization/Retro‐Mannich Cascade Reaction of N‐Aminoisoquinolinium and N‐Aminoquinolinium Derivatives with para‐Quinone Methides

Cited by 4 publications

References 48 publications

Emerging Trends for the Direct Synthesis of Dithiocarbamates

Emerging Trends for the Direct Synthesis of Dithiocarbamates

Divergent Assembly of Functionalized Pyrazolo[1,5‐a]pyridine Derivatives via [3+2] Cyclization of N‐Aminopyridinium Salts with Various Unsaturated Hydrocarbons

Recent Advances on the Construction of Functionalized Indolizine and Imidazo[1,2‐a]pyridine Derivatives

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