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Volumn 17, Issue 12, 2015, Pages 3004-3007

Catalytic Enantioselective Ring-Opening and Ring-Closing Reactions of 3-Isothiocyanato Oxindoles and N -(2-Picolinoyl)aziridines

Author keywords

[No Author keywords available]

Indexed keywords

2,2' DIHYDROXY 1,1' BINAPHTHYL; AMINO ACID; AZIRIDINE DERIVATIVE; INDOLE DERIVATIVE; ISOTHIOCYANIC ACID DERIVATIVE; LIGAND; NAPHTHOL DERIVATIVE; OXINDOLE; PEPTIDE;

EID: 84934958381     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/acs.orglett.5b01291     Document Type: Article
Times cited : (74)

References (34)
  • 31
    • 84934956050 scopus 로고    scopus 로고
    • The Lewis acidity of the chiral ligands is analyzed by comparing the p K a values of ortho-substituted phenols on the Bordwell table: (accessed May 29, 2015).
    • The Lewis acidity of the chiral ligands is analyzed by comparing the p K a values of ortho-substituted phenols on the Bordwell table: http://www.chem.wisc.edu/areas/reich/pkatable/ (accessed May 29, 2015).
  • 34
    • 84919798226 scopus 로고    scopus 로고
    • For a review on amine-thioureas bearing multiple hydrogen-bonding donors, see
    • For a review on amine-thioureas bearing multiple hydrogen-bonding donors, see: Fang, X.; Wang, C.-J. Chem. Commun. 2015, 51, 1185
    • (2015) Chem. Commun. , vol.51 , pp. 1185
    • Fang, X.1    Wang, C.-J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.