The pyrrolo[2,1-a]isoquinoline alkaloids.

Q1 Biochemistry, Genetics and Molecular Biology Alkaloids: Chemistry and Biology Pub Date : 2011-01-01 DOI:10.1016/b978-0-12-391426-2.00002-5
Ulrike Pässler, Hans-Joachim Knölker
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引用次数: 20

Abstract

The present chapter describes isolation, biogenetic proposals, and syntheses of the natural products 1-4 and 10-11 with a pyrrolo[2,1-a]-isoquinoline framework. Moreover, the syntheses of some structural analogs are discussed. The pyrrolo[2,1-a]isoquinolines are of interest due to their promising biological activities. For crispine A (1), many total syntheses have been reported and for trolline (3), only three. Only one total synthesis has been reported for each of the following natural products: peyoglutam (10), mescalotam (11), and the antitumor active crispine B (2). Some of the pyrrolo[2,1-a]isoquinoline alkaloids have not been synthesized yet. The following three tables summarize the synthetic efforts toward crispine A (1) (Table 1: racemic syntheses; Table 2: enantioselective syntheses) and trolline (3) (Table 3).

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pyrrolo[2.1 -a]同位素生物碱。
本章描述了以吡咯[2,1-a]-异喹啉为框架的天然产物1-4和10-11的分离、生物遗传学建议和合成。此外,还讨论了一些结构类似物的合成。吡咯[2,1-a]异喹啉类化合物因其具有良好的生物活性而备受关注。对于crispine A(1),有许多全合成的报道,而对于trolline(3),只有3个。以下天然产物仅报道了一次全合成:peyoglutam (10), mescalotam(11)和抗肿瘤活性crispine B(2)。一些吡咯[2,1-a]异喹啉生物碱尚未合成。以下三张表总结了crispine A的合成成果(1)(表1:外消旋合成;表2:对映选择性合成)和trolline(3)(表3)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Alkaloids: Chemistry and Biology
Alkaloids: Chemistry and Biology Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
13.70
自引率
0.00%
发文量
21
期刊最新文献
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