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Journal ArticleDOI

Polarized ethylene. V. Synthesis of 1-substituted indolizine, pyrazolo[1,5-a]pyridine, and their related compounds using methoxyethylene derivatives

TLDR
The reaction of pyridinium or isoquinolinium N-ylides with methoxy-substituted ethylenes gave the corresponding indolizine and pyrrolo[2,1-a]isoquinoline derivatives bearing acetyl, aroyl, cyano, ester group at the 1-position in one step as mentioned in this paper.
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This article is published in Journal of Heterocyclic Chemistry.The article was published on 1990-02-01. It has received 32 citations till now. The article focuses on the topics: Indolizine & Isoquinoline.

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Citations
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Journal ArticleDOI

3‐Ethyl 1‐methyl pyrrolo[2,1‐a]isoquinoline‐1,3‐dicarboxylate

TL;DR: In this article, the pyrrolo[2,1-a]isoquinoline unit is planar and the crystal structure is stabilized by weak intra-and inter-molecular C-H⋯O inter-actions, and also by π-π inter-action with centroid-centroid distances of 3.5680-3.6683
Patent

Indolizine derivative and preparation method thereof

TL;DR: In this article, an indolizine derivative and a preparation method of a cheap copper compound is taken as a catalyst, a pyridine derivative, an olefinic derivative, and a heavy nitrogen derivative are taken as reactants, and the catalyst and the reactants are subjected to cyclization reaction in a mixed solvent.
References
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Journal ArticleDOI

Molecular Orbital Theory of Orientation in Aromatic, Heteroaromatic, and Other Conjugated Molecules

TL;DR: In this article, the LCAO MO treatment of the orientation problem in chemical reactions of π-electron systems is subjected to an extension in the sense that the frontier orbitals are specified according to the type of reaction.
Journal ArticleDOI

Synthesis of Indolizine Derivatives and Their Related Compounds Using Ketene Dithioacetals

TL;DR: The synthesis of indolizine derivatives and their related compounds using ketene dithioacetals is described in this paper, where the 1, 5-dipolar cyclization is used.
Journal ArticleDOI

1,3‐Dipolare Cycloadditionen, 84. Additionen mit Chinolinium‐, Isochinolinium‐ und Phenanthridinium‐N‐imid2)

TL;DR: In this article, the reactivity of heteroaromatic N-imides and their dimers is discussed, and it is shown that the dimers behave as expected for aromatic azomethine imines as 1,3-dipoles.
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