메뉴 건너뛰기




Volumn 11, Issue 11, 2009, Pages 2317-2320

Anti-Oligoannelated THF moieties: Synthesis via push-pull-substituted cyclopropanes

Author keywords

[No Author keywords available]

Indexed keywords


EID: 66149175448     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol900694m     Document Type: Article
Times cited : (87)

References (63)
  • 1
    • 66149176842 scopus 로고    scopus 로고
    • de Meijere, A.; Khlebnikov, A. F.; Kozhushkov, S. I.; Miyazawa, K.; Frank, D.; Schreiner, P. R.; Rinderspacher, B. C.; Yufit, D. S.; Howard, J. A. K. Angew. Chem. 2004, 116, 6715-6719; Angew. Chem., Int. Ed. 2004, 43, 6553-6557.
    • de Meijere, A.; Khlebnikov, A. F.; Kozhushkov, S. I.; Miyazawa, K.; Frank, D.; Schreiner, P. R.; Rinderspacher, B. C.; Yufit, D. S.; Howard, J. A. K. Angew. Chem. 2004, 116, 6715-6719; Angew. Chem., Int. Ed. 2004, 43, 6553-6557.
  • 3
  • 4
    • 66149190605 scopus 로고    scopus 로고
    • Choi, H. S.; Kim, K. S. Angew. Chem. 1999, 111, 2400-2402; Angew. Chem., Int. Ed. 1999, 38, 2256-2258.
    • Choi, H. S.; Kim, K. S. Angew. Chem. 1999, 111, 2400-2402; Angew. Chem., Int. Ed. 1999, 38, 2256-2258.
  • 15
    • 66149186773 scopus 로고    scopus 로고
    • Morimoto, Y.; Okita, T.; Kambara, H. Angew. Chem. 2009, 121, 2576-2579; Angew. Chem. Int. Ed. 2009, 48, 2538-2541.
    • Morimoto, Y.; Okita, T.; Kambara, H. Angew. Chem. 2009, 121, 2576-2579; Angew. Chem. Int. Ed. 2009, 48, 2538-2541.
  • 16
    • 33748231608 scopus 로고    scopus 로고
    • Koert, U.; Stein, M.; Harms, K. Angew. Chem. 1994, 106, 1238- 1240. Angew. Chem. Int. Ed. Engl. 1994, 33, 1180-1182.
    • Koert, U.; Stein, M.; Harms, K. Angew. Chem. 1994, 106, 1238- 1240. Angew. Chem. Int. Ed. Engl. 1994, 33, 1180-1182.
  • 28
    • 66149179047 scopus 로고    scopus 로고
    • For recent reviews on donor-acceptor-substituted cyclopropanes
    • For recent reviews on donor-acceptor-substituted cyclopropanes: Rei-ig, H.-U.; Zimmer, R. Chem. Re V. 2003, 103, 1151-1196.
    • Chem. Re , vol.2003 , Issue.103 , pp. 1151-1196
    • Rei1    ig, H.-U.2    Zimmer, R.3
  • 52
    • 66149174821 scopus 로고    scopus 로고
    • The asymmetric diastereomer 13b was also converted to the tetraacetal 14; however, a significantly lower yield (7%) was obtained (under unoptimized conditions).
    • The asymmetric diastereomer 13b was also converted to the tetraacetal 14; however, a significantly lower yield (7%) was obtained (under unoptimized conditions).
  • 53
    • 66149192324 scopus 로고    scopus 로고
    • Due to solubility problems of the larger oligoacetals, work-up is very difficult and may be the reason for the lower yields of 17 and 20.
    • Due to solubility problems of the larger oligoacetals, work-up is very difficult and may be the reason for the lower yields of 17 and 20.
  • 54
    • 19444375335 scopus 로고    scopus 로고
    • The diffractometer was equipped with a copper rotating anode (17) or a molybdenum micro source (14). Diffraction data of structure 14 also allowed an invariom refinement which led to significant improvements in the figures of merit and the physical significance of the anisotropic displacement parameters (ADPs). For the method of invariom refinement see: Dittrich, B.; Hübschle, C. B.; Messerschmidt, M.; Kalinowski, R.; Girnt, D.; Luger, P. Acta Crystallogr. 2005, A61, 314-320.
    • The diffractometer was equipped with a copper rotating anode (17) or a molybdenum micro source (14). Diffraction data of structure 14 also allowed an invariom refinement which led to significant improvements in the figures of merit and the physical significance of the anisotropic displacement parameters (ADPs). For the method of invariom refinement see: Dittrich, B.; Hübschle, C. B.; Messerschmidt, M.; Kalinowski, R.; Girnt, D.; Luger, P. Acta Crystallogr. 2005, A61, 314-320.
  • 55
    • 66149163003 scopus 로고    scopus 로고
    • Hopf, H. Angew. Chem. 2003, 115, 2928-2932; Angew. Chem. Int. Ed. 2003, 42, 2822-2825.
    • Hopf, H. Angew. Chem. 2003, 115, 2928-2932; Angew. Chem. Int. Ed. 2003, 42, 2822-2825.
  • 57
    • 66149176841 scopus 로고    scopus 로고
    • Gao, X.; Friščic', T.; MacGillivray, L. R. Angew. Chem. 2004, 116, 234-238; Angew. Chem. Int. Ed. 2004, 43, 232-236.
    • Gao, X.; Friščic', T.; MacGillivray, L. R. Angew. Chem. 2004, 116, 234-238; Angew. Chem. Int. Ed. 2004, 43, 232-236.
  • 58
    • 66149161694 scopus 로고    scopus 로고
    • Mehta, G.; Viswanath, M. B.; Sastry, G. N.; Jemmis, E. D.; Reddy, D. S. K.; Kunwar, A. C. Angew. Chem. 1992, 104, 1557-1558; Angew. Chem. Int. Ed. Engl. 1992, 31, 1488-1490.
    • Mehta, G.; Viswanath, M. B.; Sastry, G. N.; Jemmis, E. D.; Reddy, D. S. K.; Kunwar, A. C. Angew. Chem. 1992, 104, 1557-1558; Angew. Chem. Int. Ed. Engl. 1992, 31, 1488-1490.
  • 61
    • 66149184343 scopus 로고    scopus 로고
    • Hopf, H.; Greiving, H.; Jones, P. G.; Bubenitschek, P. Angew. Chem. 1995, 107, 742-744; Angew. Chem. Int. Ed. Engl. 1995, 34, 685-687.
    • Hopf, H.; Greiving, H.; Jones, P. G.; Bubenitschek, P. Angew. Chem. 1995, 107, 742-744; Angew. Chem. Int. Ed. Engl. 1995, 34, 685-687.
  • 62
    • 66149190604 scopus 로고    scopus 로고
    • Cif files have also been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-725973 (12a), CCDC-720562 (14), and CCDC-720971 (17). Copies can be obtained via email: data-request
    • Cif files have also been deposited with the Cambridge Crystallographic Data Centre as "supplementary publication no. CCDC-725973 (12a), CCDC-720562 (14), and CCDC-720971 (17)". Copies can be obtained via email: data-request
  • 63
    • 66149168609 scopus 로고    scopus 로고
    • ccdc.cam.ac.uk
    • ccdc.cam.ac.uk.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.