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Volumn 68, Issue 12, 2012, Pages 2728-2735

Enantioselective oxysulfenylation and oxyselenenylation of olefins catalyzed by chiral Brønsted acids

Author keywords

Desymmetrization; Enantioselective; Selenenylation; Seleniranium ions; Sulfenylation; Thiiranium ions

Indexed keywords

(DEC 4 EN 1 YL)BENZENESULFENATE; 2 [1 (PHENYLTHIO)DECYL]TETRAHYDROFURAN; 2 [1 (PHENYLTHIO)ETHYL]TETRAHYDROFURAN; 2 [1 (PHENYLTHIO)HEXYL]TETRAHYDROFURAN; 2 [1 (PHENYLTHIO)PROPYL]TETRAHYDROFURAN; 2 [2,2 DIMETHYL 1 (PHENYLTHIO)PROPYL]TETRAHYDROFURAN; 2 [3 PHENYL 1 (PHENYLTHIO)PROPYL]TETRAHYDROFURAN; ALKENE DERIVATIVE; BETA CARBOXYL; BRONSTED ACID; CARBOXYL GROUP; DIBENZOYL DEXTRO TARTARIC ACID; DIBENZOYL DEXTRO TARTARIC ACID MONO 1,2;4,5 DI O ISOPROPYLIDENE BETA DEXTRO FRUCTOPYRANOSYL ESTER; DIBENZOYL LEVO TARTARIC ACID MONO 1,2;4,5-DI O ISOPROPYLIDENE BETA DEXTRO FRUCTOPYRANOSYL ESTER; SELENIDE; TARTARIC ACID DERIVATIVE; THREO 1 CYCLOHEXYL 1 (PROPYLTHIO)PROPAN 2 YL BENZOATE; THREO 5 (PROPYLTHIO)OCTAN 4 YL BENZOATE; TRAN 2 (PHENYLSELENO)CYCLOHEXYL BENZOATE; TRANS 1 BENZYLOXY 2 PHENYLTHIOCYCLOHEXANE; TRANS 1 BENZYLOXY 2 PROPYLTHIOCYCLOHEXANE; TRANS 1 ISOPROPOXY 2 PROPYLTHIOCYCLOHEXANE; TRANS 1 PHENOXY 2 PROPYLTHIOCYCLOHEXANE; TRANS 2 (BENZYLTHIO)CYCLOHEXYL BENZOATE; TRANS 2 (PHENYLSELENO)CYCLOHEXYL BENZOATE; TRANS 2 (PHENYLSELENO)CYCLOPENTYL BENZOATE; TRANS 2 (PROPYLTHIO)CYCLOHEXYL 2,6 DIMETHYL BENZOATE; TRANS 2 (PROPYLTHIO)CYCLOHEXYL ACETATE; TRANS 2 (PROPYLTHIO)CYCLOHEXYL BENZOATE; TRANS 2 (PROPYLTHIO)CYCLOPENTYL BENZOATE; UNCLASSIFIED DRUG;

EID: 84862812892     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.01.006     Document Type: Article
Times cited : (82)

References (56)
  • 5
    • 77955207631 scopus 로고    scopus 로고
    • For a leading reference on chiral sulfur and selenium reagent-mediated reactions, see
    • For a leading reference on chiral sulfur and selenium reagent-mediated reactions, see: F.W. Bürgler, G. Fragale, and T. Wirth ARKIVOC 2007 21
    • (2007) ARKIVOC , pp. 21
    • Bürgler, F.W.1    Fragale, G.2    Wirth, T.3
  • 6
    • 0000054841 scopus 로고    scopus 로고
    • For a leading review on chiral selenium reagent-mediated reactions, see
    • For a leading review on chiral selenium reagent-mediated reactions, see: T. Wirth Angew. Chem., Int. Ed. 39 2000 3740
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3740
    • Wirth, T.1
  • 26
    • 69949112440 scopus 로고    scopus 로고
    • For a leading reference on studies of stability of thiiranium ions, see
    • For a leading reference on studies of stability of thiiranium ions, see: S.E. Denmark, W.R. Collins, and M.D. Cullen J. Am. Chem. Soc. 131 2009 3490
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 3490
    • Denmark, S.E.1    Collins, W.R.2    Cullen, M.D.3
  • 27
    • 57349134538 scopus 로고    scopus 로고
    • For a leading reference on chiral anion-mediated asymmetric ring opening of meso-episulfonium ions generated from β-alkylthio trichloroacetimidate, see
    • For a leading reference on chiral anion-mediated asymmetric ring opening of meso-episulfonium ions generated from β-alkylthio trichloroacetimidate, see: G.L. Hamilton, T. Kanai, and F.D. Toste J. Am. Chem. Soc. 130 2008 14984
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 14984
    • Hamilton, G.L.1    Kanai, T.2    Toste, F.D.3
  • 30
    • 33749058561 scopus 로고    scopus 로고
    • For a leading reference on mechanistic study of selenolactonization, see
    • For a leading reference on mechanistic study of selenolactonization, see: S.E. Denmark, and M.G. Edwards J. Org. Chem. 71 2006 7293
    • (2006) J. Org. Chem. , vol.71 , pp. 7293
    • Denmark, S.E.1    Edwards, M.G.2
  • 47
  • 48
    • 79952149352 scopus 로고    scopus 로고
    • For a leading reference on asymmetric opening of meso-halonium ions, see
    • For a leading reference on asymmetric opening of meso-halonium ions, see: U. Hennecke, C.H. Müller, and R. Fröhlich Org. Lett. 13 2011 860
    • (2011) Org. Lett. , vol.13 , pp. 860
    • Hennecke, U.1    Müller, C.H.2    Fröhlich, R.3
  • 49
    • 70749161701 scopus 로고    scopus 로고
    • For a leading reference on chiral phosphoric acid-catalyzed desymmetrization of meso-aziridines, see
    • For a leading reference on chiral phosphoric acid-catalyzed desymmetrization of meso-aziridines, see: S.E. Larson, J.C. Baso, G. Li, and J.C. Antilla Org. Lett. 11 2009 5186
    • (2009) Org. Lett. , vol.11 , pp. 5186
    • Larson, S.E.1    Baso, J.C.2    Li, G.3    Antilla, J.C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.