CONFORMATION AND ABSOLUTE STEREOCHEMISTRY OF MACROCALYXOFORMIN D (= LONGIRABDIOL)

被引：9

作者：

KIDO, M

ICHIHARA, T

OTSUKA, H

TAKEDA, Y

机构：

[1] UNIV TOKUSHIMA, FAC PHARMACEUT SCI, TOKUSHIMA 770, JAPAN

[2] UNIV TOKUSHIMA, FAC INTEGRATED ARTS & SCI, TOKUSHIMA 770, JAPAN

[3] HIROSHIMA UNIV, SCH MED, INST PHARMACEUT, HIROSHIMA 734, JAPAN

来源：

CHEMICAL & PHARMACEUTICAL BULLETIN | 1992年 / 40卷 / 12期

关键词：

MACROCALYXOFORMIN-D; LONGIRABDIOL; 6,7-SECO-ENT-KAURENOID; CONFORMATION; ABSOLUTE STEREOCHEMISTRY; NUCLEAR MAGNETIC RESONANCE; X-RAY ANALYSIS; CIRCULAR DICHROISM; RABDOSIA-LONGITUBA;

D O I：

10.1248/cpb.40.3324

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

The conformation and the absolute stereochemistry of macrocalyxoformin D (=longirabdiol) was determined based on nuclear magnetic resonance spectroscopy, X-ray crystallographic analysis and circular dichroism spectroscopy.

引用

页码：3324 / 3326

页数：3

共 7 条

[1] FUJI K, 1989, CHEM PHARM BULL, V37, P1465, DOI 10.1248/cpb.37.1465
[2] HARA H, 1972, Journal of Japanese Botany, V47, P193
[3] TERPENOIDS .3. ENOLIZATION-KETONIZATION AND OPTICAL ROTATORY DISPERSION OF ENT-KAURAN-15-ONES AND 13-BETA-KAURAN-15-ONES
MACMILLAN, J
WALKER, ERH
[J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1972, (07): : 986 - +
[4] 3 NEW ANTI-TUMOR DITERPENOIDS, TRICHORABDAL-A, TRICHORABDAL-C, AND TRICHORABDAL-D
NODE, M
SAI, M
FUJI, K
FUJITA, E
SHINGU, T
WATSON, WH
GROSSIE, D
[J]. CHEMISTRY LETTERS, 1982, (12) : 2023 - 2026
[5] NODE M, 1984, HETEROCYCLES, V22, P1701
[6] TAKEDA Y, 1988, 16TH INT S CHEM NAT, P119
[7] WANG Z-Q, 1985, Acta Botanica Sinica, V27, P171

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