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Volumn 76, Issue 9, 2011, Pages 3266-3273

Experimental and computational exploration of indolizinyl carbene generation. A route to Biindolizines

Author keywords

[No Author keywords available]

Indexed keywords

BIINDOLIZINES; CARBENES; COMPUTATIONAL EXPLORATION; CYCLOPROPANATION; ELECTROSTATIC INTERACTIONS; ETHYL ACRYLATES; ONE-POT REACTION; STEREO-SELECTIVE; TRANSITION STATE;

EID: 79955569390     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo200157q     Document Type: Article
Times cited : (7)

References (63)
  • 55
    • 79955559991 scopus 로고    scopus 로고
    • note
    • This point was confirmed by obtaining 2,3-dimethyl-3-butenol upon heating dimethylbutene at 50 °C in the presence of oxygen.
  • 59
    • 0008378817 scopus 로고
    • 3-Substituted indolizines easily protonate at the C1 position: Armarego, W. L. F. J. Chem. Soc. B 1966, 191
    • (1966) J. Chem. Soc. B , pp. 191
    • Armarego, W.L.F.1
  • 62
    • 84976582072 scopus 로고
    • Biindolizine 7 had been previously obtained as a side product in our Sonogashira conditions toward Z -1-TMS
    • Biindolizine 7 had been previously obtained as a side product in our Sonogashira conditions toward Z -1-TMS: Kreher, T.; Sonnenschein, H.; Schmidt, L.; Hünig, S. Liebigs Ann. Chem. 1994, 1173
    • (1994) Liebigs Ann. Chem. , pp. 1173
    • Kreher, T.1    Sonnenschein, H.2    Schmidt, L.3    Hünig, S.4
  • 63
    • 79955564293 scopus 로고    scopus 로고
    • note
    • This relatively high activation barrier implies that the cyclization reaction operates under the Curtin-Hammett regime and, therefore, the rich conformational space of bispyridine 8 is kinetically irrelevant.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.