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Volumn 10, Issue 19, 2008, Pages 4331-4334

N-heterocyclic carbene-catalyzed oxidation of unactivated aldehydes to esters

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALDEHYDE; CARBENE; DRUG DERIVATIVE; ESTER; METHANE;

EID: 55449090881     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol8018488     Document Type: Article
Times cited : (202)

References (45)
  • 5
    • 28844466070 scopus 로고    scopus 로고
    • For a review of tandem oxidation processes, see
    • For a review of tandem oxidation processes, see: Taylor, R. J. K.; Reid, M.; Foot, J.; Raw, S. A. Acc. Chem. Res. 2005, 38, 851-869.
    • (2005) Acc. Chem. Res , vol.38 , pp. 851-869
    • Taylor, R.J.K.1    Reid, M.2    Foot, J.3    Raw, S.A.4
  • 6
    • 53849129886 scopus 로고    scopus 로고
    • For examples, see: a
    • For examples, see: (a) Ekoue-Kovi, K.; Wolf, C. Chem.-Eur. J. 2008, 14, 6302-6315.
    • (2008) Chem.-Eur. J , vol.14 , pp. 6302-6315
    • Ekoue-Kovi, K.1    Wolf, C.2
  • 31
    • 61349089940 scopus 로고    scopus 로고
    • 2 (see Table 2, entry 7).
    • 2 (see Table 2, entry 7).
  • 33
    • 61349195928 scopus 로고    scopus 로고
    • Substitution of A with 1,3-bis(2,4,6-trimethylphenyl)imidazolium chloride resulted in only partial conversion (∼25%) of the aldehyde, with significant decomposition under the standard reaction conditions.
    • Substitution of A with 1,3-bis(2,4,6-trimethylphenyl)imidazolium chloride resulted in only partial conversion (∼25%) of the aldehyde, with significant decomposition under the standard reaction conditions.
  • 34
    • 61349148771 scopus 로고    scopus 로고
    • The use of water in these reactions currently does not provide high yields of the corresponding carboxylic acid. Investigations to understand this observation and apply this new oxidation for the synthesis of carboxylic acids are underway
    • The use of water in these reactions currently does not provide high yields of the corresponding carboxylic acid. Investigations to understand this observation and apply this new oxidation for the synthesis of carboxylic acids are underway.
  • 38
    • 0038018728 scopus 로고    scopus 로고
    • Following the procedure of Foot, J. S.; Kanno, H.; Giblin, G. M. P.; Taylor, R. J. K. Synthesis 2003, 1055-1064. (Chemical Equation Presented)
    • Following the procedure of Foot, J. S.; Kanno, H.; Giblin, G. M. P.; Taylor, R. J. K. Synthesis 2003, 1055-1064. (Chemical Equation Presented)
  • 42
    • 0033515510 scopus 로고    scopus 로고
    • Zhao, M. Z.; Li, J.; Mano, E.; Song, Z. G.; Tschaen, D. M.; Grabowski, E. J. J.; Reider, P. J. J. Org. Chem. 1999, 64, 2564-2566, Subjecting 3-(2,4,6-trimethoxyphenyl)propanal to Pinnick oxidation conditions resulted in significant chlorinations of the aromatic ring. See the Supporting Information for details. (Chemical Equation Presented)
    • (c) Zhao, M. Z.; Li, J.; Mano, E.; Song, Z. G.; Tschaen, D. M.; Grabowski, E. J. J.; Reider, P. J. J. Org. Chem. 1999, 64, 2564-2566, Subjecting 3-(2,4,6-trimethoxyphenyl)propanal to Pinnick oxidation conditions resulted in significant chlorinations of the aromatic ring. See the Supporting Information for details. (Chemical Equation Presented)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.