TRANS-RING-FUSED BICYCLIC STRUCTURES BY 6-EXO-TRIGONAL RADICAL CLOSURE - USE OF THE TRIETHYLBORANE STANNANE AIR SYSTEM FOR INTRAMOLECULAR RADICAL-ADDITION TO ALDEHYDES
Selenium-containing aldehydes of type 5 are easily made by alkylation of bicyclic lactones 1, and they undergo 6-exo-trigonal radical cyclization on treatment with triphenyltin hydride in the presence of triethylborane and air to give products convertible into trans ring-fused bicyclic ketones 7.
机构:
STATE UNIV GRONINGEN,DEPT ORGAN CHEM,NIJENBORGH 16,9747 AG GRONINGEN,NETHERLANDSSTATE UNIV GRONINGEN,DEPT ORGAN CHEM,NIJENBORGH 16,9747 AG GRONINGEN,NETHERLANDS
DEJONG, JC
;
FERINGA, BL
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STATE UNIV GRONINGEN,DEPT ORGAN CHEM,NIJENBORGH 16,9747 AG GRONINGEN,NETHERLANDSSTATE UNIV GRONINGEN,DEPT ORGAN CHEM,NIJENBORGH 16,9747 AG GRONINGEN,NETHERLANDS
机构:
STATE UNIV GRONINGEN,DEPT ORGAN CHEM,NIJENBORGH 16,9747 AG GRONINGEN,NETHERLANDSSTATE UNIV GRONINGEN,DEPT ORGAN CHEM,NIJENBORGH 16,9747 AG GRONINGEN,NETHERLANDS
DEJONG, JC
;
FERINGA, BL
论文数: 0引用数: 0
h-index: 0
机构:
STATE UNIV GRONINGEN,DEPT ORGAN CHEM,NIJENBORGH 16,9747 AG GRONINGEN,NETHERLANDSSTATE UNIV GRONINGEN,DEPT ORGAN CHEM,NIJENBORGH 16,9747 AG GRONINGEN,NETHERLANDS