An efficient method of synthesis of isoxazolidine-fused β-lactams via base-promoted cyclization-ring opening of carbamoyl-spirocyclopropane isoxazolidines

Tetrahedron

Volumn 69, Issue 25, 2013, Pages 5173-5177

  Tran, Tung Q ^a   Savinkov, Ruslan S ^b   Diev, Vyacheslav V ^c   Starova, Galina L ^b   Molchanov, Alexander P ^b  

^a HANOI UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Viet Nam)

^b ST PETERSBURG STATE UNIVERSITY   (Russian Federation)

^c UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

Lactam; 1,3 Dipolar cycloaddition; Isoxazolidine; Methylenecyclopropane; Nitrone; Stereoselectivity

Indexed keywords

BETA LACTAM; ISOXAZOLIDINE DERIVATIVE; NITRONE; SPIRO[CYCLOPROPANE 1,4 ISOXAZOLIDINE]; UNCLASSIFIED DRUG;

ARTICLE; CYCLIZATION; CYCLOADDITION; ISOMER; PRIORITY JOURNAL; RING OPENING; SYNTHESIS;

EID: 84877738352     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.04.054     Document Type: Article

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