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Volumn , Issue 5, 2007, Pages 686-703

Design of highly functional small-molecule catalysts and related reactions based on acid-base combination chemistry

Author keywords

Acid base combination chemistry; Asymmetric synthesis; Catalysis; Conjugate; Salt

Indexed keywords

2 PHENYLCYCLOHEXANONE; ACROLEIN DERIVATIVE; ALCOHOL DERIVATIVE; ALKANESULFONIC ACID; ALKANONE; ALKENE; AMIDE; BRONSTED ACID; HEPTANE; HISTIDINE; LEWIS ACID; LITHIUM N HEXYLAMIDE; METAL OXIDE; N,N DIARYLAMMONIUM PENTAFLUOROBENZENESULFONATE DERIVATIVE; ORGANOMETALLIC COMPOUND; OXAZOLINE DERIVATIVE; PHOSPHODIESTERASE I; PHOSPHORIC ACID; SULFONAMIDE; SULFONIC ACID DERIVATIVE; THIAZOLE DERIVATIVE; THIAZOLINE DERIVATIVE; UNCLASSIFIED DRUG; ZINC COMPLEX;

EID: 33947728159     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-970776     Document Type: Article
Times cited : (84)

References (71)
  • 1
    • 84890969654 scopus 로고    scopus 로고
    • Breslow, R, Ed, Wiley-VCH: Weinheim
    • Artificial Enzymes; Breslow, R., Ed.; Wiley-VCH: Weinheim, 2005.
    • (2005) Artificial Enzymes
  • 2
    • 21544444468 scopus 로고    scopus 로고
    • For examples of Lewis acid-Lewis base bifunctional asymmetric catalysis, see: Kanai, M, Kato, N, Ichikawa, E, Shibaski, M. Synlett 2005, 1491
    • For examples of Lewis acid-Lewis base bifunctional asymmetric catalysis, see: Kanai, M.; Kato, N.; Ichikawa, E.; Shibaski, M. Synlett 2005, 1491.
  • 4
    • 0001433260 scopus 로고
    • For reviews, see: a, Trost, B. M, Fleming, I, Winterfeldt, E, Eds, Pergamon: Oxford
    • For reviews, see: (a) Hayakawa, Y. In Comprehensive Organic Synthesis, Vol. 6; Trost, B. M.; Fleming, I.; Winterfeldt, E., Eds.; Pergamon: Oxford, 1991, 601-630.
    • (1991) Comprehensive Organic Synthesis , vol.6 , pp. 601-630
    • Hayakawa, Y.1
  • 6
    • 0013954717 scopus 로고    scopus 로고
    • 3N under reflux in DMF (153°C) in moderate yield (38-58%). See: Honjo, M.; Furukawa, Y.; Kobayashi, K. Chem. Pharm. Bull. 1966, 14, 1061.
    • 3N under reflux in DMF (153°C) in moderate yield (38-58%). See: Honjo, M.; Furukawa, Y.; Kobayashi, K. Chem. Pharm. Bull. 1966, 14, 1061.
  • 11
    • 0034634399 scopus 로고    scopus 로고
    • Hamium(IV) and zirconium(IV) salts (0.10-1.0 mol%) are highly effective catalysts for the ester condensation reaction of carboxylic acids with equimolar amounts of alcohols. In their method azeotropic reflux conditions with the removal of water are required to form the corresponding ester in excellent yield. See: (a) Ishihara, K.; Ohara, S.; Yamamoto, H. Science 2000, 390, 1140.
    • Hamium(IV) and zirconium(IV) salts (0.10-1.0 mol%) are highly effective catalysts for the ester condensation reaction of carboxylic acids with equimolar amounts of alcohols. In their method azeotropic reflux conditions with the removal of water are required to form the corresponding ester in excellent yield. See: (a) Ishihara, K.; Ohara, S.; Yamamoto, H. Science 2000, 390, 1140.
  • 17
    • 33947721853 scopus 로고    scopus 로고
    • We have observed the similar unusual rate-accelerating effect in the dehydrative cyclization of 1,3,5-triketones to γ-pyrones catalyzed by bulky diarylammonium pentafluorobenzenesulfonates. These results more strongly suggested a hydrophobic effect of catalysts. See: Sakakura, A.; Watanabe, H.; Nakagawa, S.; Ishihara, K.; to be submitted
    • We have observed the similar unusual rate-accelerating effect in the dehydrative cyclization of 1,3,5-triketones to γ-pyrones catalyzed by bulky diarylammonium pentafluorobenzenesulfonates. These results more strongly suggested a hydrophobic effect of catalysts. See: Sakakura, A.; Watanabe, H.; Nakagawa, S.; Ishihara, K.; to be submitted
  • 19
    • 25144494141 scopus 로고    scopus 로고
    • additions and corrections
    • (b) Ishihara, K.; Nakano, K. J. Am. Chem. Soc. 2005, 127, 13079; additions and corrections.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 13079
    • Ishihara, K.1    Nakano, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.