BAEYER-VILLIGER OXIDATION OF ALKYL OXOCYCLOHEXANECARBOXYLATES

被引:14
作者
HUBERT, AJ
STARCHER, PS
机构
[1] Union Carbide Corporation, Technical Centre, South Charleston, WV 25303
来源
JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC | 1968年 / 20期
关键词
D O I
10.1039/j39680002500
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Baeyer-Villiger oxidation of methyl 3- and 4-oxocyclohexanecarboxylates gave the expected hexanolides, whereas ethyl 2-oxocyclohexanecarboxylate(I) gave 5-ethoxyoxalylpentanoic acid by way of ethyl 1-hydroxy-2- oxocyclohexanecarboxylate, formed by epoxidation of the enol form of (I).
引用
收藏
页码:2500 / &
相关论文
共 11 条
  • [1] Boeseken J, 1936, RECL TRAV CHIM PAY-B, V55, P804
  • [2] FEOFILAKTOV VV, 1945, J GEN CHEM USSR, V13, P457
  • [3] FEOFILAKTOV VV, 1941, B ACAD SCI URSS SC, P521
  • [4] OXYDATION VON ACETESSIGESTER, BENZOYLESSIGSAURE-ATHYLESTER UND DIBENZOYLMETHAN DURCH PERSAUREN
    KARRER, P
    KEBRLE, J
    THAKKAR, RM
    [J]. HELVETICA CHIMICA ACTA, 1950, 33 (06) : 1711 - 1724
  • [5] KOTZ A, 1906, ANNALEN, V350, P210
  • [6] LINDSTEAD RP, 1937, J CHEM SOC, P807
  • [7] MURPHY HW, 1943, J AMER PHARM ASSOC, P601
  • [8] PERKIN WH, 1907, J CHEM SOC, V91, P491
  • [9] ZEISS HH, 1953, J AMER CHEM SOC, V75, P900
  • [10] 1941, CA 6601