Efficient Three-Component Strecker Reaction of Aldehydes/Ketones via NHC-Amidate Palladium(II) Complex Catalysis
作者:Jamie Jarusiewicz、Yvonne Choe、Kyung Soo Yoo、Chan Pil Park、Kyung Woon Jung
DOI:10.1021/jo900163w
日期:2009.4.3
A simple and efficient one-pot, three-component method has been developed for the synthesis of α-aminonitriles. This Streckerreaction is applicable for aldehydes and ketones with aliphatic or aromatic amines and trimethylsilyl cyanide in the presence of a palladium Lewis acid catalyst in dichloromethane solvent at room temperature.
A quick and highly efficient, one-pot, three-component, solvent-free method for the synthesis of α-aminonitriles starting from the corresponding carbonyl compounds, amines, and trimethylisocyanide using triphenylphosphine dibromide, has been developed. Diverse α-aminonitriles have been synthesized in good to excellent yields (80–99%) using a range of aldehydes, ketones and amines.
A Facile Approach to Catalyst-Free Cyanation and Azidation of Organic Compounds and a One-Pot Preparation of 5-Substituted 1H-Tetrazoles by Using a Dimethyl Sulfoxide–Nitric Acid Combination
作者:Mohammad Ali Nasseri、Seyyedeh Ameneh Alavi、Boshra Mahmoudi、Milad Kazemnejadi
DOI:10.1055/s-0039-1690742
日期:2019.12
hydroxy(dimethyl)-λ4-sulfanecarbonitrile or azido(dimethyl)-λ4-sulfanol, respectively, prepared in situ by treatment of potassium cyanide or sodium azide with a dimethyl sulfoxide–nitric acid combination. Furthermore, a one-pot preparation of 5-substituted 1H-tetrazole derivatives was carried out by using this reagent combination in the presence of an aldehyde, hydroxylamine hydrochloride, and sodium azide under
Mechanochemical Strecker Reaction: Access to α-Aminonitriles and Tetrahydroisoquinolines under Ball-Milling Conditions
作者:José G. Hernández、Mathias Turberg、Ingo Schiffers、Carsten Bolm
DOI:10.1002/chem.201603057
日期:2016.10.4
Strecker reaction for the synthesis of α‐aminonitriles was developed. The milling of aldehydes, amines, and potassiumcyanide in the presence of SiO2 gave the corresponding α‐aminonitriles in good to high yields. The high efficiency of the mechanochemical Strecker‐type multicomponent reaction allowed the one‐pot synthesis of tetrahydroisoquinolines after a subsequent internal N‐alkylation reaction.
cyanide to the in situ formed imines. A comparative study of the 31P-NMR (NuclearMagneticResonance) along with IR (Infrared) data analysis for the Kraft lignin and methylated Kraft lignin samples ascertained the importance of the free hydroxyl groups in the activation of the mechanochemical reaction. The solvent-free mechanochemical Strecker reaction was then coupled with a lactamization process leading