메뉴 건너뛰기




Volumn 45, Issue 30, 2006, Pages 4988-4991

Formation of seven-membered carbocycles by the use of cyclopropyl silyl ethers as homoenols

Author keywords

Carbocycles; Cyclopropanation; Cyclopropanols; Homoenols

Indexed keywords

CARBOCYCLES; CYCLOPROPANATION; CYCLOPROPANOLS; HOMOENOLS;

EID: 33746708207     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200601011     Document Type: Article
Times cited : (30)

References (38)
  • 25
    • 0033594345 scopus 로고    scopus 로고
    • Substrates 3d, e were prepared from enantiomerically enriched 7 (> 95 % ee) by adaptation of two reported procedures: a) G. P.-J. Hareau, M. Koiwa, S. Hikichi, F. Sato, J. Am. Chem. Soc. 1999, 121, 3640;
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 3640
    • Hareau, G.P.-J.1    Koiwa, M.2    Hikichi, S.3    Sato, F.4
  • 28
    • 33746738492 scopus 로고    scopus 로고
    • We thank Dr. Mary Jane Heeg for single-crystal X-ray analysis. CCDC 280875 contains 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/products/csd/request.
  • 32
    • 0142182136 scopus 로고    scopus 로고
    • This mode of addition might be considered as a formal "edge" attack, as conformational constraints preclude "corner" attack: C. Meyer, N. Blanchard, M. Defosseux, J. Cossy, Acc. Chem. Res. 2003, 36, 766.
    • (2003) Acc. Chem. Res. , vol.36 , pp. 766
    • Meyer, C.1    Blanchard, N.2    Defosseux, M.3    Cossy, J.4
  • 33
    • 0029991524 scopus 로고    scopus 로고
    • Substrates 3g-i were prepared diastereoselectively by previously reported methods: a) J. Lee, H. Kim, J. K. Cha, J. Am. Chem. Soc. 1996, 118, 4198;
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 4198
    • Lee, J.1    Kim, H.2    Cha, J.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.