Hydroboration. 81. Synthesis of 2-(dialkylamino) boronic esters and acids via hydroboration of enamines. A convenient preparation of. beta.-dialkylamino alcohols

CT Goralski, B Singaram, HC Brown

Index: Goralski, Christian T.; Singaram, Bakthan; Brown, Herbert C. Journal of Organic Chemistry, 1987 , vol. 52, # 18 p. 4014 - 4019

Full Text: HTML

Citation Number: 34

Abstract

Hydroboration of representative enamines with 1 equiv of borane-dimethyl sulfide (BMS) in tetrahydrofuran affords as the major product the corresponding [2-(dialkylamino) alkyl] boranes, which are characterized by llB NMR spectroscopy. These intermediates on methanolysis give the corresponding [2-(diakylamino) alkyl] boronates. On treatment with water, these esters undergo rapid hydrolysis to provide the 2-[(dialkylamino) alkyl] boronic ...

Related Articles:

Microwave-enhanced bismuth triflate-catalyzed epoxide opening with aliphatic amines

[Ollevier, Thierry; Nadeau, Etienne Tetrahedron Letters, 2008 , vol. 49, # 9 p. 1546 - 1550]

Boranes in synthesis. 5. The hydroboration of enamines with mono-and dialkylboranes. asymmetric synthesis of. beta.-amino alcohols of moderate enantiomeric purity …

[Fisher, Gary B.; Goralski, Christian T.; Nicholson, Lawrence W.; Hasha, Dennis L.; Zakett, Donald; Singaram, Bakthan Journal of Organic Chemistry, 1995 , vol. 60, # 7 p. 2026 - 2034]

More Articles...