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Volumn 19, Issue 9, 2013, Pages 2961-2965

Baylis-Hillman bromides as a source of 1,3-dipoles: Sterically directed synthesis of oxindole-fused spirooxirane and spirodihydrofuran frameworks

Author keywords

cycloaddition; dipoles; fused ring systems; heterocycles; spiro compounds

Indexed keywords

[3+2]-CYCLOADDITION; BAYLIS-HILLMAN; DIPOLAROPHILES; DIPOLES; DIRECTED SYNTHESIS; FUSED-RING SYSTEM; HETEROCYCLES; OXINDOLES; SPIRO COMPOUNDS; SYNTHETIC ROUTES;

EID: 84874038232     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201203756     Document Type: Article
Times cited : (41)

References (72)
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    • CCDC-898730 (5 a), CCDC-898579 (6 a), CCDC-898580 (7 a), CCDC-898731 (6 h), CCDC-898732 (7 h), CCDC-898386 (8 d), and CCDC-898387 (8 e) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
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    • 2S and a base provided cyclopropanes; see:, K. Y. Lee, S. C. Kim, J. N. Kim, Bull. Korean Chem. Soc. 2006, 27, 319-321; similar reactions of BH-bromides with N-tosyl amines provided aziridines; see
    • (2006) Bull. Korean Chem. Soc. , vol.27 , pp. 319-321
    • Lee, K.Y.1    Kim, S.C.2    Kim, J.N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.