Title of article :
Synthesis of monocyclic nine-membered compounds by the [4+3+2] cycloaddition-bond cleavage strategy
Author/Authors :
Yamasaki، نويسنده , , Ryu and Kato، نويسنده , , Korehito and Hanitani، نويسنده , , Daichi and Mutoh، نويسنده , , Yuichiro and Saito، نويسنده , , Shinichi، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2013
Abstract :
Monocyclic nine-membered compounds were synthesized by the cleavage of the six-membered ring of the bicyclic compounds. Thus, the bicyclic compounds which consist of six- and nine-membered rings were synthesized by the Ni-catalyzed [4+3+2] cycloaddition, and the cleavage of the N–O bond, which was incorporated in the six-membered ring, proceeded in the presence of Mo(CO)6 to yield the monocyclic compound. On the other hand, the cleavage of the C–O bond proceeded efficiently in the presence of SmI2.
Keywords :
cycloaddition , Nine-Membered Carbocycle , Medium-sized ring , Reductive cleavage , Nickel catalyst , hydroxylamine , N–O bond clevage
Journal title :
Tetrahedron Letters
Journal title :
Tetrahedron Letters