Synthesis, Reactivity and Stability of Aryl Halide Protecting Groups towards Di-Substituted Pyridines | Zendy

Ptoton Mnangat Brian | Zendy; Peter Musau | Zendy

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Synthesis, Reactivity and Stability of Aryl Halide Protecting Groups towards Di-Substituted Pyridines

Author(s) -

Ptoton Mnangat Brian,

Peter Musau

Publication year - 2017

Publication title -

indonesian journal of chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.273

H-Index - 14

eISSN - 2460-1578

pISSN - 1411-9420

DOI - 10.22146/ijc.21177

Subject(s) - chemistry , halide , reactivity (psychology) , pyridinium , pyridine , aryl , ring (chemistry) , medicinal chemistry , nitrogen atom , aryl halide , derivative (finance) , organic chemistry , alkyl , medicine , alternative medicine , pathology , financial economics , economics

This paper reports the synthesis and reactivity of different Benzyl derivative protecting groups. The synthesis and stability of Benzyl halides, 4-methoxybenzyl halides, 3,5-dimethoxybenzyl halides, 3,4-dimethoxybenzyl halides, 3,4,5-trimethoxybenzyl halide protecting groups and their reactivity towards nitrogen atom of a di-substituted pyridine ring in formation of pyridinium salts is also reported.

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