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![Palladium‐Catalyzed Decarboxylative Synthesis of 5H‐Benzo[4,5][1,3]oxazino[2,3‐a]isoindole‐5,11(6aH)‐Diones using 2‐Phenyl‐4H‐Benzo[d][1,3]oxazin‐4‐Ones and α‐Oxo Carboxylic Acids - Lalji - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/93dc0677-5c69-4266-87d5-5c8cbc2ce95f/adsc201901142-toc-0001-m.jpg "Palladium‐Catalyzed Decarboxylative Synthesis of 5H‐Benzo[4,5][1,3]oxazino[2,3‐a]isoindole‐5,11(6aH)‐Diones using 2‐Phenyl‐4H‐Benzo[d][1,3]oxazin‐4‐Ones and α‐Oxo Carboxylic Acids - Lalji - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library")
Palladium‐Catalyzed Decarboxylative Synthesis of 5H‐Benzo[4,5][1,3]oxazino[2,3‐a]isoindole‐5,11(6aH)‐Diones using 2‐Phenyl‐4H‐Benzo[d][1,3]oxazin‐4‐Ones and α‐Oxo Carboxylic Acids - Lalji - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library
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An expeditious and highly efficient synthesis of substituted pyrroles using a low melting deep eutectic mixture - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D1OB01618K
![Palladium‐Catalyzed Decarboxylative Synthesis of 5H‐Benzo[4,5][1,3]oxazino[2,3‐a]isoindole‐5,11(6aH)‐Diones using 2‐Phenyl‐4H‐Benzo[d][1,3]oxazin‐4‐Ones and α‐Oxo Carboxylic Acids - Lalji - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/c212c9b9-c949-49b9-8c3b-0a931760d7f5/adsc201901142-fig-5001-m.jpg "Palladium‐Catalyzed Decarboxylative Synthesis of 5H‐Benzo[4,5][1,3]oxazino[2,3‐a]isoindole‐5,11(6aH)‐Diones using 2‐Phenyl‐4H‐Benzo[d][1,3]oxazin‐4‐Ones and α‐Oxo Carboxylic Acids - Lalji - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library")
Palladium‐Catalyzed Decarboxylative Synthesis of 5H‐Benzo[4,5][1,3]oxazino[2,3‐a]isoindole‐5,11(6aH)‐Diones using 2‐Phenyl‐4H‐Benzo[d][1,3]oxazin‐4‐Ones and α‐Oxo Carboxylic Acids - Lalji - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library
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