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Volumn 49, Issue 4, 2008, Pages 678-681

Corrigendum to "An efficient approach to the stereoselective synthesis of 2,6-disubstituted dihydropyrans via stannyl-Prins cyclization" [Tetrahedron Lett. 49 (2008) 678] (DOI:10.1016/j.tetlet.2007.11.128);An efficient approach to the stereoselective synthesis of 2,6-disubstituted dihydropyrans via stannyl-Prins cyclization

Author keywords

( ) Centrolobine; Dihydropyrans; Prins cyclization; Vinylstannanes

Indexed keywords

2,6 DIHYDROPYRAN DERIVATIVE; ION; LEWIS ACID; OXOCARBENIUM ION DERIVATIVE; PYRAN DERIVATIVE; UNCLASSIFIED DRUG; VINYLSTANNANE DERIVATIVE;

EID: 37549000198     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.12.019     Document Type: Erratum
Times cited : (42)

References (55)
  • 33
    • 37549025689 scopus 로고    scopus 로고
    • note
    • The other Lewis acids generally did not exhibit reactivity compared to that of TMSOTf, furnishing the same product, but in appreciably lower yields.
  • 34
    • 37549060916 scopus 로고    scopus 로고
    • note
    • 2O 98:2).
  • 53
    • 37449035088 scopus 로고    scopus 로고
    • note
    • Crystallographic data for structure 11 in this Letter have been deposited with the Cambridge Crystallographic Data Centre as Supplementary Publication Number CCDC 662516. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: +44 1223 336033 or e-mail: deposit@ccdc.com.ac.uk].
  • 55
    • 37549050438 scopus 로고    scopus 로고
    • note
    • 3Na, 335.1618; found, 335.1603.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.