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Volumn 22, Issue 23, 2011, Pages 2039-2055

Enantioselective α-tosyloxylation of ketones catalyzed by spirobiindane scaffold-based chiral iodoarenes

Author keywords

[No Author keywords available]

Indexed keywords

1 (3 NITROPHENYL) 1 OXOPROPAN 2 YL 4 METHYLBENZENESULFONATE; 1 (4 METHOXYPHENYL) 1 OXOPROPAN 2 YL 4 METHYLBENZENESULFONATE; 1 (4 NITROPHENYL) 1 OXOPROPAN 2 YL 4 METHYLBENZENESULFONATE; 1 (FURAN 2 YL) 1 OXOPROPAN 2 YL 4 METHYLBENZENESULFONATE; 1 (NAPHTHALEN 2 YL) 1 OXOPROPAN 2 YL 4 METHYLBENZENESULFONATE; 1 CYCLOHEXYL 1 OXOPROPAN 2 YL 4 METHYLBENZENESULFONATE; 1 OXO 1 (THIOPHEN 2 YL)PROPAN 2 YL 4 METHYLBENZENESULFONATE; 1 OXO 1 4 TOLYLPROPAN 2 YL 4 METHYLBENZENESULFONATE; 1 OXO 1 [3 (TRIFLUOROMETHYL)PHENYL]PROPAN 2 YL 4 METHYLBENZENESULFONATE; 1 OXO 1 PHENYLBUTAN 2 YL 4 METHYLBENZENESULFONATE; 1 OXO 1 PHENYLPENTAN 2 YL 4 METHYLBENZENESULFONATE; 1 OXO 1,2,3,4 TETRAHYDRONAPHTHALEN 2 YL 4 METHYLBENZENESULFONATE; 2 OXO 1,2 DIPHENYLETHYL 4 METHYLBENZENESULFONATE; 2 OXOCYCLOHEXYL 4 METHYLBENZENESULFONATE; 3 CHLOROPERBENZOIC ACID; 4,4 DIMETHYL 3 OXOPENTAN 2 YL 4 METHYLBENZENESULFONATE; IODINE DERIVATIVE; IODOARENE; KETONE DERIVATIVE; SPIROBIINDANE; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84862776800     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2011.12.003     Document Type: Article
Times cited : (68)

References (49)
  • 1
    • 79952167902 scopus 로고    scopus 로고
    • For recent reviews on hypervalent iodine reagents, see
    • For recent reviews on hypervalent iodine reagents, see: V.V. Zhdankin J. Org. Chem. 76 2011 1185 1197
    • (2011) J. Org. Chem. , vol.76 , pp. 1185-1197
    • Zhdankin, V.V.1
  • 6
    • 33745526818 scopus 로고    scopus 로고
    • L.F.S. Jr Molecules 11 2006 421 434
    • (2006) Molecules , vol.11 , pp. 421-434
  • 12
    • 83455208461 scopus 로고    scopus 로고
    • For a most recent highlight on chiral hypervalent iodine reagents in asymmetric reactions, see doi: 10.1002/anie.201106127
    • For a most recent highlight on chiral hypervalent iodine reagents in asymmetric reactions, see: Liang, H; Ciufolini, M, A. Angew. Chem. Int. Ed. doi: 10.1002/anie.201106127.
    • Angew. Chem. Int. Ed.
    • Liang, H.1    Ciufolini, M.A.2
  • 49
    • 0141688559 scopus 로고
    • The absolute configuration was determined by the independent synthesis of enantiomerically pure 1a from (S)-(-)-lactic acid
    • The absolute configuration was determined by the independent synthesis of enantiomerically pure 1a from (S)-(-)-lactic acid: M. Imfeld, M. Suchy, P. Vogt, P. Kucác, M. Schlageter, and E. Widmer Helv. Chim. Acta. 65 1982 1233 1241
    • (1982) Helv. Chim. Acta. , vol.65 , pp. 1233-1241
    • Imfeld, M.1    Suchy, M.2    Vogt, P.3    Kucác, P.4    Schlageter, M.5    Widmer, E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.