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A Convenient Ruthenium‐Catalysed α‐Methylation of Carbonyl Compounds using Methanol - Dang - 2016 - Advanced Synthesis & Catalysis - Wiley Online Library
The first intermolecular interrupted imino-Nazarov reaction: expeditious access to carbocyclic nucleoside analogues. - Abstract - Europe PMC
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US8044030B2 - Antibiotic macrocycle compounds and methods of manufacture and use thereof - Google Patents
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Visible Lightâ•'Initiated Catalystâ•'Free Oneâ•'Pot, Multicomponent Construction of 5â•'Substituted Indole C
Application of organocatalysis in bioorganometallic chemistry: asymmetric synthesis of multifunctionalized spirocyclic pyrazolone–ferrocene hybrids as ... - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C8QO00422F
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Different pathways in the reaction of N-(tosylmethyl)-substituted ureas, thioureas, and N′-cyanoguanidines with sodium cyanide. Synthesis of α-ureido nitriles, α-ureido amides, and hydantoin imino derivatives - ScienceDirect
Oxidative Ring Contraction of Cyclobutenes: General Approach to Cyclopropylketones including Mechanistic Insights
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Design and Synthesis of Potent in Vitro and in Vivo Anticancer Agents Based on 1-(3′,4′,5′-Trimethoxyphenyl)-2-Aryl-1 H -Imidazole | Scientific Reports
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Li, EtOH >P Meo. The products P and Q in the following sequence of reactions, are Meo (i) 03 (lequiv.) NH3(1) (ii) -78°C, MeH/MeS Me Meo. Meo MeO2C OHC COME Me Me
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WO2010014936A2 - Scalable synthetic process for making terameprocol - Google Patents
PDF) WiSE: Best-Path Selection in Wireless Multihoming Environments
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