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pro vyhledávání: '"Jesna Antony"'
Publikováno v:
Results in Chemistry, Vol 3, Iss , Pp 100224- (2021)
Nitrones perform as aldehyde surrogates in the preparation of chalcones via mechanochemical activation under solvent free condition. Aldonitrones containing electron releasing and electron withdrawing substituent on the C-aryl group exhibit different
Externí odkaz:
https://doaj.org/article/a3877c09b12c458b816c4ac48910f117
Publikováno v:
New Journal of Chemistry. 46:9825-9829
A rapid, catalyst-free, GREEN protocol for the synthesis of highly substituted 3(2H)-furanone and quinoline.
Autor:
Jesna Antony, Sumi P. Musthafa, Rakesh Natarajan, Sindhu Mathai, Karakkattu S. Devaky, John P. Rappai
We have developed a highly atom efficient synthesis of tetrasubstituted 3(2H)-furanones from easily accessible starting materials such as C,N-diarylaldonitrones and dibenzoylacetylene. Control experiments revealed that reaction of aldonitrones having
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02e13ea7f2116e395c789be12b8845d5
Publikováno v:
Results in Chemistry, Vol 3, Iss, Pp 100224-(2021)
Nitrones perform as aldehyde surrogates in the preparation of chalcones via mechanochemical activation under solvent free condition. Aldonitrones containing electron releasing and electron withdrawing substituent on the C-aryl group exhibit different