CYCLOVIOLAXANTHIN (= (3S,5R,6R,3'S,5'R,6'R)-3,6-3',6'-DIEPOXY-5,6,5',6'-TETRAHYDRO-BETA,BETA-CAROTENE-5,5'-DIOL), A NOVEL CAROTENOID FROM RED PAPRIKA (CAPSICUM-ANNUUM)

被引：34

作者：

DELI, J

MOLNAR, P

TOTH, G

BAUMELER, A

EUGSTER, CH

机构：

[1] UNIV PECS,SCH MED,INST CHEM,SZIGETI UT 12,H-7643 PECS,HUNGARY

[2] UNIV ZURICH,INST ORGAN CHEM,CH-8057 ZURICH,SWITZERLAND

来源：

HELVETICA CHIMICA ACTA | 1991年 / 74卷 / 04期

关键词：

D O I：

10.1002/hlca.19910740416

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

From red paprika (Capsicum annuum var. longum nigrum) cycloviolaxanthin was isolated as a minor carotenoid and, based on spectral data, assigned the symmetrical structure 8.

引用

页码：819 / 824

页数：6

共 17 条

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[2] SYNTHESES OF ENANTIOMERICALLY PURE VIOLAXANTHINS AND RELATED-COMPOUNDS [J].

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[4]

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[6] SYNTHESES OF OPTICALLY-ACTIVE CAROTENOIDS WITH 3,5,6-TRIHYDROXY-5,6-DIHYDRO BETA-END GROUPS [J].

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HELVETICA CHIMICA ACTA, 1984, 67 (08) :2043-2056

[7]

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[8] CAROTENOIDS WITH 7-OXABICYCLO[2.2.1]HEPTYL END GROUPS - ATTEMPTED SYNTHESIS OF CYCLOVIOLAXANTHIN (=(3S,5R,6R,3'S,5'R,6'R)-3,6-3',6'-DIEPOXY-5,6,5',6'-TETRAHYDRO-BETA,BETA-CAROTIN-5,5'-DIOL) [J].

GMUNDER, MR ;

EUGSTER, CH .

HELVETICA CHIMICA ACTA, 1990, 73 (07) :1954-1969

[9] CAROTENOIDS WITH 7-OXABICYCLO[2.2.1]HEPTYL END GROUPS .2. SYNTHESIS OF (2S,5R,6S,2'S,5'R,6'S)-2,5-2',5'-DIEPOXY-5,6,5',6'-TETRAHYDRO-BETA,BETA-CAROTENE [J].

GMUNDER, MR ;

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HELVETICA CHIMICA ACTA, 1990, 73 (08) :2190-2198

[10] NEOFLOR AND 6-EPINEOFLOR FROM FLOWERS OF TROLLIUS-EUROPAEUS - HIGHFIELD H-1-NMR SPECTRA OF (ALL-E)-NEOXANTHIN AND (9'Z)-NEOXANTHIN [J].

MARKIFISCHER, E ;

EUGSTER, CH .

HELVETICA CHIMICA ACTA, 1990, 73 (06) :1637-1643

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