A new short synthesis of deoxyhydantocidin derivatives

Tetrahedron Letters

Volumn 39, Issue 20, 1998, Pages 3129-3132

  Renard, Annabelle ^a   Kotera, Mitsuharu ^a   Lhomme, Jean ^a  

^a UNIVERSITÉ JOSEPH FOURIER   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYRIBONUCLEOSIDE;

ARTICLE; CYCLIZATION; NUCLEAR MAGNETIC RESONANCE; POLYMERIZATION; STEREOCHEMISTRY; SYNTHESIS;

EID: 0032516302     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00438-9     Document Type: Article

References (21)

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9. 4. We use the nucleoside numbering system for the hydantocidin derivatives (see figure) in reference to oligonucleotides. Similar numbering was used originally in ref 2b. According to the usual hydantoin numbering, compound 2b refers as 4-deoxyhydantocidin.
10. β has been previously described and shown to have no herbicidal activity: Mio, S.; Sano, H.; Shindou, M.; Honma, T.; Sugai, S. Agric. Biol. Chem. 1991, 55, 1105-1109.
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16. 7a.
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19. 12. Using TOCSY experiments, the components of the mixture A were fully assigned.
20. 13. The stereochemistry of 14a and 14b was not determined.
21. 2O : C 65.49, H 5.69, N 5.46; found: C 65.66, H 5.82, N 5.46.