Title of article :
Formation of 2-halomethylene-4-cyclopentene-1,3-diones and/or 2-halo-1,4-benzoquinones via ring-expansion of 4-ethynyl-4-hydroxy-2,3-substituted-2-cyclobuten-1-ones. Total synthesis of methyl linderone
Author/Authors :
Hong Yin، نويسنده , , Shubhada W. Dantale، نويسنده , , Novruz G. Akhmedov، نويسنده , , Bj?rn C.G. S?derberg، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2013
Pages :
10
From page :
9284
To page :
9293
Abstract :
An in-depth study of the reactions of 4-(ethynyl)-4-hydroxy-2,3-substituted-2-cyclobuten-1-ones with N-bromo- or N-iodosuccinimide, affording in most cases 2-halomethylene-4-cyclopentene-1,3-dione, is described. This reaction was used in a short total synthesis of methyl linderone.
Keywords :
Alkynylcyclobutenones , 2-Alkylidene-1 , 3-cyclopentendiones , rearrangement , Methyl linderone , N-halosuccinimide
Journal title :
Tetrahedron
Serial Year :
2013
Journal title :
Tetrahedron
Record number :
1106381
Link To Document :
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