SCOPUS 정보 검색 플랫폼

Volumn 35, Issue 47, 1994, Pages 8797-8800

The yellow toxins produced by Cercospora Beticola. Part VIII : Chemical equilibrium between beticolins ; structures of minor compounds : beticolin 6 and beticolin 8

(4) Ducrot, P H a Lallemand, J Y b Milat, M L c Blein, J P c

a INRA (France)

b LABORATOIRE DE SYNTHÈSE ORGANIQUE (France)

c UNIVERSITÉ DE BOURGOGNE (France)

Author keywords

[No Author keywords available]

Indexed keywords

BETICOLIN 6; BETICOLIN 8; MYCOTOXIN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; NUCLEAR MAGNETIC RESONANCE;

CERCOSPORA BETICOLA;

EID: 0027944121 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)78501-7 Document Type: Article

Times cited : (21)

References (8)

1
- 0000519733
- Structures of the beticolins, the yellow toxins produced by Cercospora beticola
- (1992) Journal of the American Chemical Society , vol.114 , pp. 1478-1479
- Milat¹ Prangé² Ducrot³ Tabet⁴ Einhorn⁵ Blein⁶ Lallemand⁷

2
- 0027537402
- The yellow toxins produced by Cercospora beticola. Part II: Isolation and structure of beticolins 3 and 4
- (1993) Tetrahedron Letters , vol.34 , pp. 1483-1486
- Milat¹ Prangé² Ducrot³ Tabet⁴ Einhorn⁵ Blein⁶ Lallemand⁷

3
- 84913001462
- accepted for publication
- (1994) J. Chem. Soc. Chem. Commun.
- Ducrot¹ Lallemand² Milat³ Blein⁴

4
- 0000060316
- Cercospora beticola phytotoxins: cebetins that are photoactive, magnesium ion-binding, chlorinated anthraquinone-xanthone conjugates
- (1992) Journal of the American Chemical Society , vol.114 , pp. 5967-5971
- Jalal¹ Hossain² Robeson³ Van⁴

5
- 37049071989
- (1993) J. Chem. Soc. C. , pp. 145-151
- Arnone¹ Nasini² Merlini³ Ragg⁴ Assante⁵

6
- 0000884199
- Triglycerides and Cercosporin from Cercospora beticola: Fungal Growth and Cercosporin Production
- 3 (400 MHz) : 15.35 (s, 1H), 14.95 (s, 1H), 12.61 (s, 1H), 12.23 (s, 1H), 11.65 (s, 1H), 7.58, 7.55 (2H J=12 Hz, H-4′, H-5′), 4.65 (dd, 1H,J=12, 5 Hz, H-3), 3.1 (ddd, 1H, J=17, 12, 5.2 Hz, H-5b), 2.64 (ddd, 1H, J=17, 5.7, 1 Hz, H-5a), 2.33 (qd, 1H, J= 12, 5.2 Hz, H-4a), 2.11 (tdd, 1H J=12, 5, 1 Hz, H-4b), 3.82 (s, 3H,H-16), 4.72 (d, 1H, H-11′, J=1.4 Hz), 4.22 (d,1H, H-13′, J=1.4 Hz), 3.57 (s, 2H, H-15′),1.68 (s,3H, H16′). [[Truncated]]
- (1971) Phytopathology , vol.61 , pp. 1477
- Balis¹ Payne²

7
- 48549112001
- (1984) J. Magn. Res. , vol.58 , pp. 370-382
- Bodenhausen¹ Kogler² Ernst³

8
- 84913008224
- 2O, J= 5Hz, OH-3), 4.55 (dt, 1H,J=12, 5 Hz, H-3), 3.05 (m, 1H, H-5b), 2.80 (ddd, 1H, J=16, 6, 1 Hz, H-5a), 2.41 (m 1H, H-4a), 2.15 (m, 1H, H-4b), 3.75 (s, 3H,H-16), 4.95 (d, 1H, H-11′, J=1.3 Hz), 4.30 (d,1H, H-13′, J=1.3 Hz), 3.35–3.55 (system AB, J=17 Hz, 2H, H-15′),3.88, 4.05 (2H, H16′).

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.