Synthesis of 5,5-diallyl-substituted oxazolidin-2-one derivatives, based on reductive diallylation of amino acids

Synthesis of 5,5-diallyl-substituted oxazolidin-2-one derivatives, based on reductive diallylation of amino acids Full article

Journal

Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285

Output data

Year: 2022, Volume: 71, Number: 3, Pages: 580-583 Pages count : 4 DOI: 10.1007/s11172-022-3452-z

Authors

Klimenko R.V. ¹ , Starykh S.A. ¹ , Baranin S.V. ¹ , Bubnov Yu.N. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

An efficient synthesis of 5,5-diallyl-substituted oxazolidinone derivatives, based on reductive diallylation of available α-amino acids, was developed. It was demonstrated that the obtained oxazolidinones can be readily converted into the corresponding derivatives of 3-azaspiro[4,4]-non-7-en-2-one via the metathesis reaction in the presence of the 1st generation Grubbs catalyst.

Klimenko R.V. , Starykh S.A. , Baranin S.V. , Bubnov Y.N.
Synthesis of 5,5-diallyl-substituted oxazolidin-2-one derivatives, based on reductive diallylation of amino acids
Russian Chemical Bulletin. 2022. V.71. N3. P.580-583. DOI: 10.1007/s11172-022-3452-z WOS Scopus OpenAlex

≡ Web of science:	WOS:000787316800024
≡ Scopus:	2-s2.0-85128822070
≡ OpenAlex:	W4224441403