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... 2023, 145, 21623-21629. DOI: 10.1021/jacs.3c07974 see article for more reactions Abstract Readily available and structurally diverse alkyl carboxylic acids can serve as the starting ...
... ,5-Bis(trifluoromethyl)phenyl]oxazaborilidine Catalyst for Use in the Mukaiyama Aldol Reaction Kazuaki Ishihara, Shoichi Kondo, Hisashi Yamamoto* *Department of Chemistry, ...
... (MeNCH2CH2)3N: A Novel Ylide for Quantitative E Selectivity in the Wittig Reaction Zhigang Wang, Guangtao Zhang, Ilia Guzei and John G. Verkade* ...
... Organic Chemistry Portal Pd/C as a Reusable Catalyst for the Coupling Reaction of Halophenols and Arylboronic Acids in Aqueous Media Hidehiro Sakurai, Tatsuya Tsukada and Toshikazu ...
... Organic Chemistry Portal Triethanolamine as an Efficient and Reusable Base, Ligand and Reaction Medium for Phosphane-Free Palladium-Catalyzed Heck Reactions Hong Ji Li, Lei Wang* *Department ...
... yields, compared to conventional heating, which is related to the elimination of side reactions. This "green chemistry" approach uses very mild basic aqueous conditions which ...
... Organic Chemistry Portal Phase-Vanishing Reactions that Use Fluorous Media as a Phase Screen. Facile, Controlled Bromination of Alkenes by Dibromine and Dealkylation of Aromatic Ethers by Boron ...
... Organic Chemistry Portal Tetraphosphine/palladium catalysed Suzuki cross-coupling reactions of aryl halides with alkylboronic acids Isabelle Kondolff , Henri Doucet* and Maurice Santelli *Laboratoire de Synthèse ...
... Organic Chemistry Portal Highly Efficient Pd-Catalyzed Carbonylative Cross-Coupling Reactions with Tetraorganoindates Sung Wook Lee, Kooyeon Lee, Dong Seomoon, Sundae Kim, Hyunseok Kim, Hyun Kim ...
... conversion of aromatic and aliphatic nitriles to the corresponding N-tert-butyl amides: a modified Ritter reaction K. Laxma Reddy* *Process Research and Development, Bristol-Myers Squibb Pharmaceutical ...
