Literature DB >> 15340193

A new synthetic method for an indolizidine skeleton by C-N bond formation via a pi-allylpalladium complex.

Yaeko Yamada1, Wakako Takahashi, Yoshihisa Asada, Junko Holiuchi, Kazuyoshi Takeda, Yoshihiro Harigaya.   

Abstract

Pd(0)-catalyzed intramolecular cyclic reaction via a pi-allylpalladium complex provided an indolizidine skeleton in satisfactory high and reproducible yields by using allylic compound having an acetoxyl group as a leaving group. These results must be available for syntheses of various functional indolizidine alkaloids.

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Year:  2004        PMID: 15340193     DOI: 10.1248/cpb.52.1082

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  1 in total

1.  Total synthesis of pumiliotoxins 209F and 251D via late-stage, nickel-catalyzed epoxide-alkyne reductive cyclization.

Authors:  Katrina S Woodin; Timothy F Jamison
Journal:  J Org Chem       Date:  2007-08-14       Impact factor: 4.354

  1 in total

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