Synthesis and Reactivity of Propargylamines in Organic Chemistry
Синтез и реакционная способность пропаргиламинов в органической химии
2017-11-22
SCID: 54.1/753rpwgs
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A3 couplingC–H functionalization of alkynesenantioselective synthesisheterocyclic compoundspropargylamines
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Abstract (AI)
Propargylamines are a versatile class of compounds which find broad application in many fields of chemistry. This review aims to describe the different strategies developed so far for the synthesis of propargylamines and their derivatives as well as to highlight their reactivity and use as building blocks in the synthesis of chemically relevant organic compounds. In the first part of the review, the different synthetic approaches to synthesize propargylamines, such as A 3 couplings and C–H functionalization of alkynes, have been described and organized on the basis of the catalysts employed in the syntheses. Both racemic and enantioselective approaches have been reported. In the second part, an overview of the transformations of propargylamines into heterocyclic compounds such as pyrroles, pyridines, thiazoles, and oxazoles, as well as other relevant organic derivatives, is presented.
Key Findings
1
Both racemic and enantioselective methods for synthesizing propargylamines and their derivatives are covered.
2
Propargylamines are versatile building blocks for preparing pyrroles, pyridines, thiazoles, oxazoles, and other chemically relevant organic derivatives.
3
The review highlights broad applications of propargylamines and summarizes their key reactivity patterns in organic synthesis.
4
The review organizes propargylamine synthesis strategies by catalyst type, including A3 couplings and alkyne C–H functionalization.
Research Object
Propargylamines (and their derivatives) as chemical building blocks
Research Subject
Synthetic strategies, reactivity, and use of propargylamines as building blocks for producing heterocyclic compounds and other chemically relevant organic derivatives
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2017-11-22
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