Azomethine ylids from diethyl aminomalonate

doi:10.1016/S0040-4039(00)82420-X

Paper

Azomethine ylids from diethyl aminomalonate

Published 1988 · S. Husinec, V. Savić, A. Porter

Tetrahedron Letters

Q3 SJR score

5

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0

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Abstract

Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.

Study Snapshot

Diethyl aminomalonate reacts with formaldehyde to form pyrrolidine derivatives, or azomethine ylids, depending on the dipolarophiles present.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Paper

Azomethine ylids from diethyl aminomalonate

References

Citations

A stereodivergent cascade imine → azomethine ylide → 1,3-dipolar cycloadditive approach to α-chiral pyrrolidines

This study presents a new approach to synthesize highly functionalized pyrrolidines, potentially offering a new approach to the bioxalomycin family of antibiotics.

Acid-induced dimerization of imidates derived from glycine: Synthesis of methylN-(1,2,5-trisubstituted-4-imidazoyl)glycinates

Acid-induced dimerization of imidates derived from glycine leads to the synthesis of N-(1,2,5-trisubstituted-4-imidazoyl)-glycinates in moderate yield.

Development of chiral stabilised azomethine ylids: A chiral memory relay system.

Chiral stabilised azomethine ylids in cyclic templates can be used to create enantioselective 1,3-dipolar cycloaddition reactions, yielding enantiomerically pure -substituted proline derivatives.