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Volumn 72, Issue 6, 2007, Pages 2106-2117

Regio- and stereospecific synthesis of β-sulfonamidodisulfides and β-sulfonamidosulfides from aziridines using tetrathiomolybdate as a sulfur transfer reagent

Author keywords

[No Author keywords available]

Indexed keywords

LEWIS ACID; SULFONAMIDODISULFIDES; SULFUR TRANSFER REAGENT; TETRATHIOMOLYBDATE;

EID: 33947270986     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0624389     Document Type: Article
Times cited : (42)

References (47)
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    • (b) Hu, X. E. Tetrahedron 2004, 60, 2701-2743.
    • (2004) Tetrahedron , vol.60 , pp. 2701-2743
    • Hu, X.E.1
  • 15
    • 33947197931 scopus 로고    scopus 로고
    • It has been tested with other protecting groups (activating groups) such as Boc and Cbz, but the reaction took more time (20 h) in the case of Boc and in the case of Cbz the reaction was incomplete even after 88 h. The N-Boc-protected 2,3-disubstituted aziridines failed to undergo ring opening with 1
    • It has been tested with other protecting groups (activating groups) such as Boc and Cbz, but the reaction took more time (20 h) in the case of Boc and in the case of Cbz the reaction was incomplete even after 88 h. The N-Boc-protected 2,3-disubstituted aziridines failed to undergo ring opening with 1.
  • 21
    • 33947257056 scopus 로고    scopus 로고
    • CCDC 631951 (5d), CCDC 631952 (7a), CCDC 631953 (7c), CCDC 631954 (9a), CCDC 631955 (9b), CCDC 288572 (9c), CCDC 631956 (11a), CCDC 631957 (14), CCDC 631958 (32), CCDC 631959 (36), and CCDC 631960 (44) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from the Cambridge Crystallography Data Centre via www.ccdc.cam.ac.uk/data request/cif.
    • CCDC 631951 (5d), CCDC 631952 (7a), CCDC 631953 (7c), CCDC 631954 (9a), CCDC 631955 (9b), CCDC 288572 (9c), CCDC 631956 (11a), CCDC 631957 (14), CCDC 631958 (32), CCDC 631959 (36), and CCDC 631960 (44) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from the Cambridge Crystallography Data Centre via www.ccdc.cam.ac.uk/data request/cif.
  • 25
    • 33947192186 scopus 로고    scopus 로고
    • Epoxide 31 was prepared from D-glucose in five steps through a known procedure: Methods in Carbohydrate Chemistry; Academic Press: New York, 1963; II, p 190.
    • (a) Epoxide 31 was prepared from D-glucose in five steps through a known procedure: Methods in Carbohydrate Chemistry; Academic Press: New York, 1963; Vol. II, p 190.
  • 36
    • 33947238518 scopus 로고    scopus 로고
    • VanRheenen, V.; Cha, D. Y.; Hartley, W. M. Organic Syntheses; Wiley: New York, 1988; Collect. VI, p 342.
    • (b) VanRheenen, V.; Cha, D. Y.; Hartley, W. M. Organic Syntheses; Wiley: New York, 1988; Collect. Vol. VI, p 342.
  • 37
    • 33947274818 scopus 로고    scopus 로고
    • Maras, A.; H. Secen, H.; Sutbeyaz, Y.; Balci, M. J. Org. Chem. 1998, 63, 2039-2041.
    • (c) Maras, A.; H. Secen, H.; Sutbeyaz, Y.; Balci, M. J. Org. Chem. 1998, 63, 2039-2041.
  • 43
    • 33947259629 scopus 로고    scopus 로고
    • DFT calculations were carried out on intermediates I and II using B3LYP method and the 6-31.G(d) level basis set using Guassian 98.
    • DFT calculations were carried out on intermediates I and II using B3LYP method and the 6-31.G(d) level basis set using Guassian 98.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.