WebChemistry and Chemical Biology Lithium amidotrihydroborate (LiH3NBH3, LAB) is a new and highly nucleophilic reducing agent that is easily prepared by deprotonation of the commercial reagent... WebLithium amidotrihydroborate (LiH3NBH3, LAB) is a new and highly nucleophilic reducing agent that is easily prepared by deprotonation of the commercial reagent borane …
Asymmetric synthesis of (+)-pyrido[3,4-b]homotropane.
Web1 Access to Enantiopure 4-Substituted 1,5-Aminoalcohols from Phenylglycinol-Derived -Lactams. Synthesis of Haliclona Alkaloids Mercedes Amat*, Guillaume Guignard, Núria Llor, and Web14 apr. 2013 · Finally, reductive removal of the chiral auxiliary with lithium amidotrihydroborate [26] produced alcohol 14, and benzylation yielded triether 15. Scheme 2: Synthesis of triether 15 . Asymmetric epoxidation of alkene 15 was somewhat sluggish and required superstoichiometric amounts of Shi’s fructose-derived ketone 16 [27]. flow simulator online
Stereoselective Formation of Quaternary Carbon Centers
Web21 dec. 2015 · Lithium aminoborohydrides (LiABH(3)) are a new class of powerful yet selective reducing agents that reproduce, in air, virtually all of the transformations for which lithium aluminum hydride is... Web(+)-Pyrido[3,4-b]homotropane (PHT) was efficiently constructed in 12 steps from N,N-diisopropylisonicotinamide. The synthesis features (i) RCM reaction in installing the … Web15 apr. 2002 · Lithium Amidotrihydroborate, a Powerful New Reductant. Transformation of Tertiary Amides to Primary Alcohols. A. Myers, Bryant H. Yang, D. J. Kopecky … flows in