Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Keijin Nakaguro"'
Publikováno v:
Organic & Biomolecular Chemistry. 20:5397-5401
A new single-step approach to a C3a acetoxy pyrroloindole from various indoles under hypervalent iodine and ammonium salt-mediated mild reaction conditions was developed. The described method enables the short-step synthesis of (−)-protubonine B.
Publikováno v:
Organicbiomolecular chemistry. 20(27)
A method for the synthesis of C3a acetoxy hexahydropyrrolo[2,3
Publikováno v:
Tetrahedron. 94:132314
In this study, we attempted to carry out the Mitsunobu 1,4-elimination using the kojic acid analog 3, which carries a hydroxymethyl group on C-6 introduced by aldol condensation, to obtain an effective Michael acceptor 4. To the ethyl acetate solutio