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Volumn , Issue 11, 2002, Pages 1850-1854

Synthesis of all carbon linked glycoside clusters round benzene scaffold via Sonogashira-Heck-Cassar cross-coupling of iodobenzenes with ethynyl C-glycosides

Author keywords

Alkynes; Clusters; Cross coupling; Sonogashira reaction; Sugar acetylenes

Indexed keywords

ALKYNE; BENZENE; CARBON; GLYCOSIDE; IODOBENZENE; PALLADIUM;

EID: 0036418006     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2002-34885     Document Type: Article
Times cited : (19)

References (41)
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    • note
    • 3)
  • 27
    • 0011322544 scopus 로고    scopus 로고
    • note
    • 5.6 = 9.7 Hz, H-5), 1.99 (d, 1 H, H-1).
  • 31
    • 0000509322 scopus 로고
    • Trost, B. M.; Fleming, I., Eds.; Pergamon Press: New York
    • For reviews, see: (a) Sonogashira, K. In Comprehensive Organic Synthesis, Vol. 3; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: New York, 1991, 521. (b) Rossi, R.; Carpita, A.; Bellina, F. Org. Prep. Proced. Int. 1995, 27, 129. (c) Tsuji, J. Palladium Reagents and Catalysts; Wiley & Sons: Chichester, 1995, 168. (d) Brandsma, L.; Vasilevsky, S. F.; Verkruijsse, H. D. Application of Transition Metal Catalysts in Organic Synthesis; Springer: Berlin, 1998, 179.
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 521
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  • 32
    • 0000471264 scopus 로고
    • For reviews, see: (a) Sonogashira, K. In Comprehensive Organic Synthesis, Vol. 3; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: New York, 1991, 521. (b) Rossi, R.; Carpita, A.; Bellina, F. Org. Prep. Proced. Int. 1995, 27, 129. (c) Tsuji, J. Palladium Reagents and Catalysts; Wiley & Sons: Chichester, 1995, 168. (d) Brandsma, L.; Vasilevsky, S. F.; Verkruijsse, H. D. Application of Transition Metal Catalysts in Organic Synthesis; Springer: Berlin, 1998, 179.
    • (1995) Org. Prep. Proced. Int. , vol.27 , pp. 129
    • Rossi, R.1    Carpita, A.2    Bellina, F.3
  • 33
    • 0003441482 scopus 로고
    • Wiley & Sons: Chichester
    • For reviews, see: (a) Sonogashira, K. In Comprehensive Organic Synthesis, Vol. 3; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: New York, 1991, 521. (b) Rossi, R.; Carpita, A.; Bellina, F. Org. Prep. Proced. Int. 1995, 27, 129. (c) Tsuji, J. Palladium Reagents and Catalysts; Wiley & Sons: Chichester, 1995, 168. (d) Brandsma, L.; Vasilevsky, S. F.; Verkruijsse, H. D. Application of Transition Metal Catalysts in Organic Synthesis; Springer: Berlin, 1998, 179.
    • (1995) Palladium Reagents and Catalysts , pp. 168
    • Tsuji, J.1
  • 34
    • 0003664601 scopus 로고    scopus 로고
    • Springer: Berlin
    • For reviews, see: (a) Sonogashira, K. In Comprehensive Organic Synthesis, Vol. 3; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: New York, 1991, 521. (b) Rossi, R.; Carpita, A.; Bellina, F. Org. Prep. Proced. Int. 1995, 27, 129. (c) Tsuji, J. Palladium Reagents and Catalysts; Wiley & Sons: Chichester, 1995, 168. (d) Brandsma, L.; Vasilevsky, S. F.; Verkruijsse, H. D. Application of Transition Metal Catalysts in Organic Synthesis; Springer: Berlin, 1998, 179.
    • (1998) Application of Transition Metal Catalysts in Organic Synthesis , pp. 179
    • Brandsma, L.1    Vasilevsky, S.F.2    Verkruijsse, H.D.3
  • 35
    • 0011323478 scopus 로고    scopus 로고
    • note
    • 8a.8b = 12.0 Hz, 2 H-8a), 3.72-3.64 (m, 2 H, 2 H-8b), 3.43-3.27 (m, 8 H).
  • 37
    • 0011282518 scopus 로고    scopus 로고
    • note
    • 14.15b = 2.2 Hz, 3 H-15b), 3.67 (ddd, 3 H, 3 H-14), 3.46-3.33 (m, 9 H, 3 H-3, 3 H-7, 3 H-10), 2.87-2.76, 2.51-2.40, 1.94-1.85, 1.77-1.68, and 1.52-1.39 (5 m, 24 H), 2.12, 2.08, 2.06, 2.02, 2.01, and 1.98 (6 s, 63 H, 21 Ac).
  • 40
    • 0011276981 scopus 로고    scopus 로고
    • note
    • 7.8b = 1.8 Hz, 4 H-8b), 3.35-3.29 (m, 4H, 4 H-7), 1.84, 1.74, 1.72, and 1.64(4s, 48 H, 16 Ac); MALDI-TOF MS: 1519.3 (M + Na), 1535.8 (M + K).
  • 41
    • 0011279371 scopus 로고    scopus 로고
    • note
    • 7.8b = 3.8 Hz, 4 H-8b), 3.23-3.12 (m, 12 H), 3.03-2.98 (m, 8 H), 2.71-2.56 (m, 8 H), 1.95-1.83 (m, 4 H), 1.60-1.46 (m, 4 H).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.