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A convenient synthesis of novel N ‐dichloroacetyl‐1,3‐oxazolidine
Author(s) -
Ye Fei,
Yang Lei,
Li Haitao,
Fu Ying,
Xu Weijun
Publication year - 2010
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.289
Subject(s) - chemistry , oxazolidine , acylation , cycloalkane , condensation , alkyl , organic chemistry , proton nmr , combinatorial chemistry , stereochemistry , catalysis , physics , thermodynamics
A short and efficient route of synthesis and structural characterization of a series of novel N ‐dichloroacetyl‐1,3‐oxazolidine derivatives has been developed. These new compounds characterized of the disubstitution at position 2 by alkyl, cycloalkane, and phenyl were synthesized in good yields via a sequential procedure involving condensation and acylation . All the compounds are characterized by IR, 1 H NMR, 13 C NMR, and element analysis. J. Heterocyclic Chem., (2010).

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