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J Org Chem ; 76(2): 534-42, 2011 Jan 21.
Article in English | MEDLINE | ID: mdl-21188968

ABSTRACT

A catalytic asymmetric allylation of 3,4-dihydroisoquinoline was carried out with allyltrimethoxylsilane-Cu as the nucleophile in the presence of DTBM-SEGPHOS as the chiral ligand to afford corresponding chiral 1-allyltetrahydroisoquinoline derivatives in good yield and stereoselectivity. The allyl adduct thus obtained was applied to the synthesis of several isoquinoline alkaloids such as crispine A and homolaudanosine. The reaction was further used for the synthesis of the isoquinoline moiety of schulzeine A.


Subject(s)
Alkaloids/chemistry , Alkaloids/chemical synthesis , Isoquinolines/chemistry , Isoquinolines/chemical synthesis , Catalysis , Copper/chemistry , Ligands , Magnetic Resonance Spectroscopy , Molecular Structure , Organosilicon Compounds/chemistry , Stereoisomerism
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