On the acylation reactions of aza-allyl carbanions derived from N-[bis(methylthio)methylene]glycine ethyl ester and N-[bis(methylthio)methylene]benzylamine

DOI: 10.1016/S0040-4020(97)00091-4

Source and publish data:

Tetrahedron p. 3679 - 3692 (1997)

Update date:2022-08-04

Topics:

Authors:

Alvarez-Ibarra, Carlos

Csaky, Aurelio G.

Martinez-Santos, Elena

Quiroga, Maria L.

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Article abstract of DOI:10.1016/S0040-4020(97)00091-4

New aspects of the acylation reaction of the aza-allyl anions derived from 1 and 2 have been studied. Under suitable reaction conditions, osazoles 5, α,α-disubstituted α-acyla-amino acid derivatives 3, and α,β-didehydroamino acid derivatives 7 can be prep

Full text of DOI:10.1016/S0040-4020(97)00091-4

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Article Doi

On the acylation reactions of aza-allyl carbanions derived from N-[bis(methylthio)methylene]glycine ethyl ester and N-[bis(methylthio)methylene]benzylamine

DOI: 10.1016/S0040-4020(97)00091-4

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4020(97)00091-4

Full text of DOI:10.1016/S0040-4020(97)00091-4

Products guided by the article

R&D Labs maybe for 185450-25-3

Relevant to this article

Novel radiosynthesis of PET HSV-tk gene reporter probes [ 18F]FHPG and [18F]FHBG employing dual Sep-Pak SPE techniques

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Synthesis of the complexes [PdClR(cod)] (R = benzyl, ethyl; cod = 1,5-cyolooctadiene). β-Elimination from [PdClEt(cod)] to give the η1,η2, and η3 isomers of [Pd2(μ-Cl)2(C8H13)2]

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