五环氧化吲哚生物碱的立体化学 - Suppr

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The stereochemistry of the pentacyclic oxindole alkaloids.

作者信息

Shamma M, Shine R J, Kompis I, Sticzay T, Morsingh F, Poisson J, Pousset J L

出版信息

J Am Chem Soc. 1967 Mar 29;89(7):1739-40. doi: 10.1021/ja00983a041.

DOI:10.1021/ja00983a041

PMID:6046541

Abstract

摘要

相似文献

The stereochemistry of the pentacyclic oxindole alkaloids.五环氧化吲哚生物碱的立体化学

J Am Chem Soc. 1967 Mar 29;89(7):1739-40. doi: 10.1021/ja00983a041.

The effect of methoxy substitution and configuration on the thin-layer chromatographic behaviour of some closed E ring oxindole alkaloids.甲氧基取代和构型对一些闭环E环氧化吲哚生物碱薄层色谱行为的影响。

J Chromatogr. 1968 Feb 20;32(4):704-14. doi: 10.1016/s0021-9673(01)80549-5.

The thin layer chromatographic behaviour of some E seco oxindole alkaloids, and their relationship with indolizidine and some simple oxindoles.一些E-裂环氧化吲哚生物碱的薄层色谱行为及其与吲哚里西啶和一些简单氧化吲哚的关系。

J Chromatogr. 1968 Feb 20;32(4):692-703. doi: 10.1016/s0021-9673(01)80548-3.

The quantitative determination of some mitragyna oxindole alkaloids after separation by thin-layer chromatograppy. I. Ultraviolet spectrophotometry.薄层色谱分离后某些帽柱木吲哚生物碱的定量测定。I. 紫外分光光度法。

J Chromatogr. 1968 Feb 6;32(3):472-88. doi: 10.1016/s0021-9673(01)80520-3.

The correlation between the stereochemistry of some indole and oxindole alkaloids and their behaviour on thin layer chromatograms.

J Chromatogr. 1966 Sep;24(1):84-92. doi: 10.1016/s0021-9673(01)98104-x.

[Stereochemistry of oxindole alkaloids].[氧化吲哚生物碱的立体化学]

Bull Soc Chim Fr. 1967 Aug;8:2766-79.

[Research on the skytanthine series. 3. Stereochemistry of the alkaloids of Skytanthus acutus].[刺唐松草碱系列研究。3. 尖叶唐松草生物碱的立体化学]

Ann Ist Super Sanita. 1965;1(1):257-62.

[The helical nature of oxindole alkaloids: a new notation].

Tetrahedron Lett. 1967 May;20:1919-23. doi: 10.1016/s0040-4039(00)90755-x.

The quantitative determination of some mitragyna oxindole alkaloids after separation by thin-layer chromatography. IV. Comparison of ultra-violet spectrophotometry, colorimetry and densitometry as methods for the quantitative determination of oxindole alkaloids in plant material.

J Chromatogr. 1968 May 21;35(1):72-82. doi: 10.1016/s0021-9673(01)82351-7.

Functional divergency oriented synthesis of azoninones as the key intermediates for bioactive indolizidine alkaloids analogs.以氮杂环辛酮为导向的功能发散性合成，作为生物活性吲哚里西啶生物碱类似物的关键中间体。

Arch Pharm Res. 2004 Oct;27(10):985-9. doi: 10.1007/BF02975418.

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Gold Catalyzed Multicomponent Reactions beyond A³ Coupling.金催化的三元以上偶联反应

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Rauniticine-allo-oxindole B and rauniticinic-allo acid B, new heteroyohimbine-type oxindole alkaloids from the stems of Malaysian Uncaria longiflora var. pteropoda.马来西亚钩藤茎中的新异育亨宾型吲哚生物碱——劳尼定全-β-阿朴-8,19-二去甲氧基酸 B 和劳尼定全-β-阿朴-8-甲氧基酸 B。

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