期刊
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
卷 339, 期 1-2, 页码 32-36出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.molcata.2011.02.008
关键词
Optically active oxetanes; Chiral 1,4-aminoalcohols; Hydrogenolysis; Catalytic hydrogenation; Palladium; Solvent effects
资金
- CNR (Firenze)
- Hungarian Academy of Sciences
- New Hungary Development Plan [TAMOP-4.2.1/B-09/1/KMR-2010-0002]
An efficient method for the palladium mediated hydrogenation of an optically active, N-protected aminooxetane derivative has been developed. Using appropriate solvents, in a one-step reaction, a chiral 1,4-aminoalcohol derivative [(2S,3R)-4-amino-3-benzoyloxy-2-benzylbutan-1-ol] was formed over a Pd/C catalyst, during hydrogenolytic ring opening and debenzylation reactions. (C) 2011 Elsevier B.V. All rights reserved.
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