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Volumn 77, Issue 8, 2012, Pages 4005-4016

A palladium iodide-catalyzed carbonylative approach to functionalized pyrrole derivatives

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLIC SOLVENTS; ALKYNYL GROUPS; ALKYNYLS; ARYL SUBSTITUENTS; CARBONYLATION REACTIONS; CATALYTIC SYSTEM; DIASTEREOMERIC; DIASTEREOMERS; ESTER DERIVATIVES; FUNCTIONALIZED; HYDROXYL GROUPS; MOLAR RATIO; ONE STEP; PYRROLE DERIVATIVES; REACTION CONDITIONS; REGIO-SELECTIVE; WATER ADDITION; X-RAY CRYSTALLOGRAPHIC ANALYSIS;

EID: 84860161292     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo300365n     Document Type: Article
Times cited : (51)

References (81)
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    • Guo, X.; Zhu, Z. (Allergen, Inc.) U.S. Pat. US2011053905A1, 2011.
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    • Guo, X.1    Zhu, Z.2
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    • Yuan, J.; Ma, D.; Zhang, L. (Harvard College and Shanghai Institute of Organic Chemistry) World Pat. WO2009049242A1, 2009.
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    • Yuan, J.1    Ma, D.2    Zhang, L.3
  • 47
    • 84860170882 scopus 로고    scopus 로고
    • (King's College London) World Pat. WO2008087421A2
    • Amobi, N. I.; Smith, C. (King's College London) World Pat. WO2008087421A2, 2008.
    • (2008)
    • Amobi, N.I.1    Smith, C.2
  • 48
    • 84860133579 scopus 로고    scopus 로고
    • (The General Hospital Corporation and Northeastern University) World Pat. WO2008066576A2
    • Ausubel, F. M.; Lewis, K.; Moy, T.; Gopalan, S. (The General Hospital Corporation and Northeastern University) World Pat. WO2008066576A2, 2008.
    • (2008)
    • Ausubel, F.M.1    Lewis, K.2    Moy, T.3    Gopalan, S.4
  • 73
    • 0003574131 scopus 로고    scopus 로고
    • These conditions (16 atm of CO together with 5 total atm of air, considering that the autoclave was loaded under 1 atm of air) corresponded to 76.2% of CO in air and were outside the explosion limits for CO in air, which are ca. 16-70% at 18-20 °C and atmospheric pressure, 14.8-71.4% at 100 °C and atmospheric pressure; at higher total pressure, the range of flammability decreases: for example, at 20 atm and 20 °C, the limits are ca. 19 and 60%. See: Bartish, C. M.; Drissel, G. M. In Kirk-Othmer Encyclopedia of Chemical Technology, 3 rd ed.
    • Kirk-Othmer Encyclopedia of Chemical Technology
    • Bartish, C.M.1    Drissel, G.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.