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OZONOLYSES OF ISOPHORONE AND OF 3-METHYL-2-CYCLOHEXEN-1-ONE AND SUBSEQUENT REACTIONS OF THE RESPECTIVE OZONIDES TO AFFORD DI-, TRI- AND TETRAOZONIDES

  作者 JUNG IN CHAN; SHEIKH SAD ALAM; JON BYONGMUN; LI WEI; GOO BONSUK; JEONG INSOO  
  选自 期刊  Heterocycles;  卷期  2010年81-10;  页码  2323-2334  
  关联知识点  
 

[摘要]Ozonolyses of isophorone (1a) and 3-methyl-2-cyclohexen-1-one (1b) in pentane, followed by treatment of the ozonolyses products with O-methyl-hydroxylamine afforded the ozonides 3,3,5-Trimethyl-6,7,8-trioxabicycle[3.2.1] octane-1 -carbaldehyde-O-methyloxime (5a) and 5-Methyl-6,7,8-trioxabicyclo [3.2.1]octane-1-carbaldehyde-O-methyloxime (5b), respectively. Coozonolyses of ozonides 5 with selected carbonyl compounds resulted in the formation of diozonides (9, 11), triozonides (12) and tetraozonides (14).

 
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