Mycaperoxides F and G and a related norterpene ketone from southern Australian marine sponges, Mycale species

被引：21

作者：

Capon, RJ ^{[1
]}

Rochfort, SJ

Ovenden, SPB

Metzger, RP

机构：

[1] Univ Melbourne, Dept Chem, Parkville, Vic 3052, Australia

[2] San Diego State Univ, Dept Chem, San Diego, CA 92182 USA

来源：

JOURNAL OF NATURAL PRODUCTS | 1998年 / 61卷 / 04期

关键词：

D O I：

10.1021/np970484l

中图分类号：

Q94 [植物学];

学科分类号：

071001 ;

摘要：

Investigation of two southern Australian marine sponges, Mycale spp., resulted in isolation of the known norsesterterpene mycaperoxide F methyl ester (5) together with a new norsesterterpene mycaperoxide G methyl ester (10) and a new norterpene ketone 11. All structures were secured by spectroscopic analysis and chemical derivatization. The absolute stereochemistry previously assigned to 5 by application of the Horeau procedure has been revised by application of the Mosher procedure.

引用

页码：525 / 528

页数：4

共 10 条

[1] THE LUFFARINS (A-Z), NOVEL TERPENES FROM AN AUSTRALIAN MARINE SPONGE, LUFFARIELLA-GEOMETRICA [J].

BUTLER, MS ;

CAPON, RJ .

AUSTRALIAN JOURNAL OF CHEMISTRY, 1992, 45 (10) :1705-1743

[2] NORTERPENE DIENES FROM AN AUSTRALIAN MARINE SPONGE LATRUNCULIA-BREVIS [J].

BUTLER, MS ;

CAPON, RJ .

AUSTRALIAN JOURNAL OF CHEMISTRY, 1991, 44 (01) :77-85

[3] 2 NEW NORSESTERTERPENE CYCLIC PEROXIDES FROM A MARINE SPONGE, MYCALE (CARMIA) CF SPONGIOSA [J].

CAPON, RJ .

JOURNAL OF NATURAL PRODUCTS, 1991, 54 (01) :190-195

[4] Cyclic peroxides and related norterpenes from a southern Australian marine sponge, Mycale sp. [J].

Capon, RJ ;

Rochfort, SJ ;

Ovenden, SPB .

JOURNAL OF NATURAL PRODUCTS, 1997, 60 (12) :1261-1264

[5] STRUCTURAL AND STEREOCHEMICAL STUDIES ON MARINE NORTERPENE CYCLIC PEROXIDES [J].

CAPON, RJ ;

MACLEOD, JK .

TETRAHEDRON, 1985, 41 (16) :3391-3404

[6] STRUCTURAL AND STEREOCHEMICAL STUDIES ON MARINE NORTERPENE CYCLIC PEROXIDES .2. [J].

CAPON, RJ ;

MACLEOD, JK .

JOURNAL OF NATURAL PRODUCTS, 1987, 50 (02) :225-229

[7]

CAPON RJ, UNPUB

[8] NUCLEAR MAGNETIC-RESONANCE ENANTIOMER REAGENTS - CONFIGURATIONAL CORRELATIONS VIA NUCLEAR MAGNETIC-RESONANCE CHEMICAL-SHIFTS OF DIASTEREOMERIC MANDELATE, O-METHYLMANDELATE, AND ALPHA-METHOXY-ALPHA-TRIFLUOROMETHYLPHENYLACETATE (MTPA) ESTERS [J].

DALE, JA ;

MOSHER, HS .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1973, 95 (02) :512-519

[9] Parguerenes revisited: New brominated diterpenes from the southern Australian marine red alga Laurencia filiformis [J].

Rochfort, SJ ;

Capon, RJ .

AUSTRALIAN JOURNAL OF CHEMISTRY, 1996, 49 (01) :19-26

[10] BIOACTIVE NORSESTERTERPENE 1,2-DIOXANES FROM A THAI SPONGE, MYCALE SP [J].

TANAKA, J ;

HIGA, T ;

SUWANBORIRUX, K ;

KOKPOL, U ;

BERNARDINELLI, G ;

JEFFORD, CW .

JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (11) :2999-3002

← 1 →