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Volumn 42, Issue 47, 2003, Pages 5838-5843

(-)-Daucic Acid: Revision of Configuration, Synthesis, and Biosynthetic Implications

Author keywords

Carbohydrates; Chelidonic acid; Configuration determination; Daucic acid; Osbeckic acid

Indexed keywords

BIOSYNTHESIS; CARBON; OXIDATION; SYNTHESIS (CHEMICAL);

EID: 0348050488     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200352718     Document Type: Article
Times cited : (19)

References (30)
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    • note
    • 2.3 = 7.5 Hz. Consequently, these data are not useful for comparative purposes.
  • 9
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    • a) Acetylation and bromination: R. W. Jeanloz, P. J. Stoffyn, Methods Carbohydr. Chem. 1962, 1, 224-225; J. Conchie, G. A. Levy, Methods Carbohydr. Chem. 1963, 2, 336;
    • (1962) Methods Carbohydr. Chem. , vol.1 , pp. 224-225
    • Jeanloz, R.W.1    Stoffyn, P.J.2
  • 10
    • 0347611164 scopus 로고
    • a) Acetylation and bromination: R. W. Jeanloz, P. J. Stoffyn, Methods Carbohydr. Chem. 1962, 1, 224-225; J. Conchie, G. A. Levy, Methods Carbohydr. Chem. 1963, 2, 336;
    • (1963) Methods Carbohydr. Chem. , vol.2 , pp. 336
    • Conchie, J.1    Levy, G.A.2
  • 11
    • 0345147106 scopus 로고
    • b) HBr elimination: K. Maurer, A. Müller, Ber. Dtsch. Chem. Ges. A 1930, 63, 2069-2073. When purification of the two intermediates is avoided, an overall yield of 75% is observed for the three steps.
    • (1930) Ber. Dtsch. Chem. Ges. A , vol.63 , pp. 2069-2073
    • Maurer, K.1    Müller, A.2
  • 14
    • 84980124739 scopus 로고
    • a) E. Fischer, B. Oetker, Ber. Dtsch. Chem. Ges. 1913, 46, 4029-4040; R. K. Irani, J. L. Bose, Indian J. Chem. 1975, 13, 529;
    • (1975) Indian J. Chem. , vol.13 , pp. 529
    • Irani, R.K.1    Bose, J.L.2
  • 16
    • 0027512468 scopus 로고
    • N. J. Davis, S. L. Flitsch, Tetrahedron Lett. 1993, 34, 1181-1184; A. E. J. de Nooy, A. C. Besemer, H. van Bekkum, Recl. Trav. Chim. Pays-Bas 1995, 51, 8023-8032; Z. Györgydeák, J. Thiem, Carbohydr. Res. 1995, 268, 85-92.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 1181-1184
    • Davis, N.J.1    Flitsch, S.L.2
  • 18
    • 0028951075 scopus 로고
    • N. J. Davis, S. L. Flitsch, Tetrahedron Lett. 1993, 34, 1181-1184; A. E. J. de Nooy, A. C. Besemer, H. van Bekkum, Recl. Trav. Chim. Pays-Bas 1995, 51, 8023-8032; Z. Györgydeák, J. Thiem, Carbohydr. Res. 1995, 268, 85-92.
    • (1995) Carbohydr. Res. , vol.268 , pp. 85-92
    • Györgydeák, Z.1    Thiem, J.2
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    • note
    • Dictum attributed to Sir Robert Robinson.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.