Literature DB >> 17315932

General synthesis of pyrroloquinolizidines: synthesis of an unnatural homologue of the pyrroloindolizidine myrmicarin alkaloid 215B.

Steven R Angle1, Xuelei Lily Qian, Alexandre A Pletnev, Jason Chinn.   

Abstract

A general synthesis approach to pyrroloquinolizidines (3,4,5,5a,6,7,8-heptahydropyrrolo[2,1,5-de]quinolizines) via a münchnone 1,3-dipolar cycloaddition is reported. The approach was applied to the synthesis of an unnatural pyrroloquinolizidine homologue of myrmicarin 215B.

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Year:  2007        PMID： 17315932     DOI： 10.1021/jo062262a

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


  3 in total

1.  A neutral polydisulfide containing Gd(III) DOTA monoamide as a redox-sensitive biodegradable macromolecular MRI contrast agent.

Authors:  Zhen Ye; Zhuxian Zhou; Nadia Ayat; Xueming Wu; Erlei Jin; Xiaoyue Shi; Zheng-Rong Lu
Journal:  Contrast Media Mol Imaging       Date:  2015-07-27       Impact factor: 3.161

2.  Novel benzothiophene 1,1-dioxide deoxygenation path for the microwave-assisted synthesis of substituted benzothiophene-fused pyrrole derivatives.

Authors:  Hamza Karakuş; Yaşar Dürüst
Journal:  Mol Divers       Date:  2016-09-27       Impact factor: 2.943

3.  Total synthesis and study of myrmicarin alkaloids.

Authors:  Alison E Ondrus; Mohammad Movassaghi
Journal:  Chem Commun (Camb)       Date:  2009-05-19       Impact factor: 6.222
  3 in total

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