Carboran (Romanian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Carboran" in Romanian language version.

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  • Eluvathingal D. Jemmis (). „Overlap control and stability of polyhedral molecules. Closo-Carboranes”. J. Am. Chem. Soc. 104: 7017–7020. doi:10.1021/ja00389a021. 
  • Mark Juhasz, Stephan Hoffmann, Evgenii Stoyanov, Kee-Chan Kim, Christopher A. Reed (). „The Strongest Isolable Acid”. Angewandte Chemie International Edition. 43: 5352–5355. doi:10.1002/anie.200460005. 
  • Christopher A. Reed (). „Carborane acids. New "strong yet gentle" acids for organic and inorganic chemistry” (PDF). Chem. Commun. 2005: 1669–1677. doi:10.1039/b415425h. Arhivat din original (Full article (reprint)) la . Accesat în . 
  • Kutal, C. R.; Owen, D. A.; Todd, L. J. (). „Closo-1,2-dicarbadodecaborane(12)”. Inorganic Syntheses. 11: 19–23. doi:10.1002/9780470132425.ch5. 
  • T. L. Heying, J. W. Ager, S. L. Clark, D. J. Mangold, H. L. Goldstein, M. Hillman, R. J. Polak, and J. W. Szymanski (). „A New Series of Organoboranes. I. Carboranes from the Reaction of Decaborane with Acetylenic Compounds”. Inorganic Chemistry. 2: 1089–1092. doi:10.1021/ic50010a002. 
  • H. Schroeder, T. L. Heying, J. R. Reiner (). „A New Series of Organoboranes. II. The Chlorination of 1,2-Dicarbaclosododecaborane(12)" Inorganic Chemistry”. Inorganic Chemistry. 2: 1092–1096. doi:10.1021/ic50010a003. 
  • T. L. Heying, J. W. Ager, S. L. Clark, R. P. Alexander, S. Papetti, J. A. Reid, S. I. Trotz (). „A New Series of Organoboranes. III. Some Reactions of 1,2-Dicarbaclosododecaborane(12) and its Derivatives”. Inorganic Chemistry. 2: 1097–1105. doi:10.1021/ic50010a004.  Text " Inorganic Chemistry " ignorat (ajutor)
  • S. Papetti, T. L. Heying (). „A New Series of Organoboranes. IV. The Participation of the 1,2-Dicarbaclosododecaborane(12) Nucleus in Some Novel Heteratomic Ring Systems”. Inorg. Chem. 2: 1105–1107. doi:10.1021/ic50010a005. 
  • M. M. Fein, J. Bobinski, N. Mayes, N. Schwartz, M. S. Cohen (). „Carboranes. I. The Preparation and Chemistry of 1-Isopropenylcarborane and its Derivatives (a New Family of Stable Closoboranes)”. Inorg. Chem. 2: 1111–1115. doi:10.1021/ic50010a007. 
  • M. M. Fein, D. Grafstein, J. E. Paustian, J. Bobinski, B. M. Lichstein, N. Mayes, N. N. Schwartz, M. S. Cohen (). „Carboranes. II. The Preparation of 1- and 1,2-Substituted Carboranes”. Inorg. Chem. 2: 1115–1119. doi:10.1021/ic50010a008. 
  • D. Grafstein, J. Bobinski, J. Dvorak, H. Smith, N. Schwartz, M. S. Cohen, M. M. Fein (). „Carboranes. III. Reactions of the Carboranes”. Inorg. Chem. 2: 1120–1125. doi:10.1021/ic50010a009. 
  • D. Grafstein, J. Bobinski, J. Dvorak, J. E. Paustian, H. F. Smith, S. Karlan, C. Vogel, M. M. Fein (). „Carboranes. IV. Chemistry of Bis-(1-carboranylalkyl) Ethers”. Inorg. Chem. 2: 1125–1128. doi:10.1021/ic50010a010. .
  • D. Grafstein, J. Dvorak (). „Neocarboranes, a New Family of Stable Organoboranes Isomeric with the Carboranes”. Inorg. Chem. 2: 1128–1133. doi:10.1021/ic50010a011. 
  • Henry L. Gingrich, Tirthankar Ghosh, Qiurong Huang, and Maitland Jones (). „1,2-Dehydro-o-carborane”. J. Am. Chem. Soc. 112 (10): 4082–4083. doi:10.1021/ja00166a080. 
  • E. D. Jemmis and B. Kiran (). „Structure and Bonding in B10X2H10 (X = C and Si). The Kinky Surface of 1,2-Dehydro-o-Disilaborane”. J. Am. Chem. Soc. 119 (19): 4076–4077. doi:10.1021/ja964385q. 
  • B. Kiran, A. Anoop, E. D. Jemmis (). „Control of Stability through Overlap Matching: closo-Carboranes and closo-Silaboranes”. J. Am. Chem. Soc. 124: 4402–4407. doi:10.1021/ja016843n. 
  • Liang Deng, Hoi-Shan Chan, and Zuowei Xie (). „Nickel-Mediated Regioselective [2 + 2 + 2] Cycloaddition of Carboryne with Alkynes”. J. Am. Chem. Soc. 128 (24): 7728–7729. doi:10.1021/ja061605j. 

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