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Volumn 8, Issue 1, 1997, Pages 23-26

Chiral hypervalent iodine compounds

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; IODINE DERIVATIVE; ORGANOIODINE DERIVATIVE;

EID: 0031016525     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(96)00469-7     Document Type: Article
Times cited : (109)

References (33)
  • 2
    • 0345246271 scopus 로고
    • Ed. Waldmann, H., VCH, Weinheim
    • b) Waldmann, H. in Organic Synthesis Highlights II, Ed. Waldmann, H., VCH, Weinheim, 1995, 223-230;
    • (1995) Organic Synthesis Highlights , vol.2 , pp. 223-230
    • Waldmann, H.1
  • 18
    • 0000855362 scopus 로고
    • a) Wirth, T. Angew. Chem. 1995, 107, 1872-1873; Angew. Chem. Int. Ed. Engl. 1995, 34, 1726-1728;
    • (1995) Angew. Chem. , vol.107 , pp. 1872-1873
    • Wirth, T.1
  • 19
    • 33748219016 scopus 로고
    • a) Wirth, T. Angew. Chem. 1995, 107, 1872-1873; Angew. Chem. Int. Ed. Engl. 1995, 34, 1726-1728;
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 1726-1728
  • 21
    • 0342961512 scopus 로고    scopus 로고
    • Diploma thesis, Universität Basel 2-Iodobenzoylchloride was treated with chiral alcohols (borneol) or amines (phenylalanine methylester; 1-phenylethylamine) to yield the corresponding esters resp. amides, which were then transformed into the hypervalent hydroxy(tosyloxy)iodo compounds. In the reactions mentioned in the text no selectivities were obtained with these reagents
    • Hirt, U. H. Diploma thesis, Universität Basel 1996. 2-Iodobenzoylchloride was treated with chiral alcohols (borneol) or amines (phenylalanine methylester; 1-phenylethylamine) to yield the corresponding esters resp. amides, which were then transformed into the hypervalent hydroxy(tosyloxy)iodo compounds. In the reactions mentioned in the text no selectivities were obtained with these reagents.
    • (1996)
    • Hirt, U.H.1
  • 26
    • 0343396919 scopus 로고    scopus 로고
    • note
    • 5.
  • 27
    • 0342961511 scopus 로고    scopus 로고
    • Institut für Anorganische Chemie der Universität Basel
    • Neuburger-Zehnder, M.; Neuburger, M. Institut für Anorganische Chemie der Universität Basel.
    • Neuburger-Zehnder, M.1    Neuburger, M.2
  • 31
    • 0028272208 scopus 로고
    • Compound 7 was found to have 80% ee
    • 3SnH, AIBN) was compared with the literature value (Seebach, D.; Beck, A. K.; Schmidt, B.; Wang, Y. M. Tetrahedron 1994, 50, 4363-4368). Compound 7 was found to have 80% ee.
    • (1994) Tetrahedron , vol.50 , pp. 4363-4368
    • Seebach, D.1    Beck, A.K.2    Schmidt, B.3    Wang, Y.M.4
  • 33
    • 0001415581 scopus 로고
    • The absolute configuration was determined by the synthesis of 11 and 12 from (S)-mandelic acid: Dale, J. A.; Mosher, H. S. J. Org. Chem. 1970, 35, 4002-4003.
    • (1970) J. Org. Chem. , vol.35 , pp. 4002-4003
    • Dale, J.A.1    Mosher, H.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.