Synthesis of model tricyclic C-O-D-O-E-F-O-G ring of teicoplanin

Tetrahedron Letters

Volumn 38, Issue 33, 1997, Pages 5795-5798

  Bois Choussy, Michèle ^a   Vergne, Caroline ^a   Neuville, Luc ^a   Beugelmans, René ^a   Zhu, Jieping ^a  

^a INSTITUT DE CHIMIE DES SUBSTANCES NATURELLES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

TEICOPLANIN;

ARTICLE; DRUG SYNTHESIS; IN VITRO STUDY; METHODOLOGY; MODEL; REACTION ANALYSIS; STEREOCHEMISTRY; TEMPERATURE;

EID: 0030878383     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)01280-X     Document Type: Article

References (28)

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26. 3CN, 400 MHz) δ: 8.21 (d, J = 2.0 Hz, 1H), 8.20 (d, J = 2.0 Hz, 1H), 7.90 (d, J = 8.2 Hz, 1H), 7.44 (dd, J = 2.0, 8.5 Hz, 1H), 7.2-7.4 (m, 7H), 7.08 (dd, J = 2.0, 8.8 Hz, 1H), 7.05 (d, J = 8.7 Hz, 1H), 6.8-7.0 (m, 5H), 6.82 (d, J = 8.8 Hz, 2H), 6.65 (brs, 1H), 6.15 (s, 1H), 5.78 (s, 1H), 5.47 (d, J = 10.1 Hz, 1H), 5.16 (d, J = 9 Hz, 1H), 5.0 (d, J = 7.6 Hz, 1H), 4.79 (m, 1H), 4.09 (m, 1H), 4.0 (s, 3H), 3.90 (d, J = 14.8 Hz, 1H), 3.76 (s, 3H), 3.62 (d, J = 14.8 Hz, 1H), 3.61 (s, 3H), 3.45 (dd, J = 5.4, 14.1 Hz, 1H), 3.05 (dd, J = 3.4, 14.1 Hz, 1H), 2.78 (dd, J = 7.4, 14.1 Hz); FABMS: 1081 (M +1); mp: >330°C.
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