Asymmetric Aldol Reaction of α‐Acetoxyimino Aldehydes and its Application in the Synthesis of Substituted 1,2‐Oxazine Derivatives - Yasui - 2014 - Advanced Synthesis & Catalysis - Wiley Online Library
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Iridium-Catalyzed C–H Borylation of CF3-Substituted Pyridines | ACS Omega
Di-bromo-Based Small-Molecule Inhibitors of the PD-1/PD-L1 Immune Checkpoint | Journal of Medicinal Chemistry
Asymmetric Aldol Reaction of α‐Acetoxyimino Aldehydes and its Application in the Synthesis of Substituted 1,2‐Oxazine Derivatives - Yasui - 2014 - Advanced Synthesis & Catalysis - Wiley Online Library
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IJMS | Free Full-Text | First X-ray Crystal Structure Characterization, Computational Studies, and Improved Synthetic Route to the Bioactive 5-Arylimino-1,3,4-thiadiazole Derivatives
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IJMS | Free Full-Text | First X-ray Crystal Structure Characterization, Computational Studies, and Improved Synthetic Route to the Bioactive 5-Arylimino-1,3,4-thiadiazole Derivatives
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Iridium-Catalyzed C–H Borylation of CF3-Substituted Pyridines | ACS Omega
Total Synthesis of the Proposed Structure of the Anthrapyran Metabolite δ‐Indomycinone - Tietze - 2007 - Chemistry – A European Journal - Wiley Online Library
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Total Synthesis of the Proposed Structure of the Anthrapyran Metabolite δ‐Indomycinone - Tietze - 2007 - Chemistry – A European Journal - Wiley Online Library
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IJMS | Free Full-Text | First X-ray Crystal Structure Characterization, Computational Studies, and Improved Synthetic Route to the Bioactive 5-Arylimino-1,3,4-thiadiazole Derivatives
Total Synthesis of the Proposed Structure of the Anthrapyran Metabolite δ‐Indomycinone - Tietze - 2007 - Chemistry – A European Journal - Wiley Online Library
Iridium-Catalyzed C–H Borylation of CF3-Substituted Pyridines | ACS Omega
Synthesis, structure and evaluation of anticancer activity of 4-amino-1,3-thiazolinone/pyrazoline hybrids - ScienceDirect
