கரிமபோரான் வேதியியல் (Tamil Wikipedia)

Analysis of information sources in references of the Wikipedia article "கரிமபோரான் வேதியியல்" in Tamil language version.

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11doi.org

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3acs.org

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1inist.fr

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1iupac.org

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acs.org

pubs.acs.org

Miyaura, Norio; Suzuki, Akira (1995). "Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds". Chemical Reviews 95 (7): 2457–2483. doi:10.1021/cr00039a007. http://pubs.acs.org/doi/abs/10.1021/cr00039a007.
Bethany Halford Boron Attacks Electropositive element pressed into action as nucleophilic boryllithium Chemical & Engineering News 2006; Volume 84(41): 11 Link
Neutral Diborene Is A First Ron Dagani Chemical & Engineering News October 1, 2007 Volume 85, Number 40 p. 10 [1]

doi.org

dx.doi.org

Negishi, E.-i.; Idacavage, M. J. Org. React. 1985, 33, 1. எஆசு:10.1002/0471264180.or033.01
Lachance H., Hall D. (2008). "Allylboration of Carbonyl Compounds". Org. React. 73: 1. doi:10.1002/0471264180.or073.01.
Nicolaou, K.C.; Sarabia, F.; Ninkovic, S.; Finlay, M.R.V.; Boddy, C.N.C. (1998). "Probing The Ring Size Of Epothilones: Total Synthesis Of 14-, 15-, 17-, And 18 Epothilones A". Angewandte Chemie International Edition in English 37 (1–2): 81–84. doi:10.1002/(sici)1521-3773(19980202)37:1/2<81::aid-anie81>3.0.co;2-c. http://cat.inist.fr/?aModele=afficheN&cpsidt=10349604. பார்த்த நாள்: 2008-03-02.
Vedejs E., Chapman R. W., Fields S. C., Lin S., Schrimpf M. R. (1995). "Conversion of Arylboronic Acids into Potassium Aryltrifluoroborates: Convenient Precursors of Arylboron Difluoride Lewis Acids". J. Org. Chem. 60 (10): 3020–3027. doi:10.1021/jo00115a016.
Molander Gary A., Canturk Belgin (2009). "Organotrifluoroborates and Monocoordinated Palladium Complexes as Catalysts—A Perfect Combination for Suzuki–Miyaura Coupling". Angew. Chem. Int. Ed. 48: 9240–9261. doi:10.1002/anie.200904306.
Batey Robert A., Quach Tan D., Shen Ming, Thadani Avinash N., Smil David V., Li Sze-Wan, MacKay D. Bruce (2002). "Organoboron compounds as mild nucleophiles in Lewis acid- and transition metal-catalyzed C–C bond-forming reactions" (PDF). Pure Appl. Chem. 74 (1): 43–55. doi:10.1351/pac200274010043. http://www.iupac.org/publications/pac/2002/pdf/7401x0043.pdf.
Miyaura, Norio; Suzuki, Akira (1995). "Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds". Chemical Reviews 95 (7): 2457–2483. doi:10.1021/cr00039a007. http://pubs.acs.org/doi/abs/10.1021/cr00039a007.
Segawa Yasutomo, Yamashita Makoto, Nozaki Kyoko (2006). "Boryllithium: Isolation, Characterization, and Reactivity as a Boryl Anion". Science 314 (5796): 113–115. doi:10.1126/science.1131914.
Paetzold Peter, Englert Ulli, Finger Rudolf, Schmitz Thomas, Tapper Alexander, Ziembinski Ralf (2004). "Reactions at the Boron-Carbon Double Bond of Methyl(methylidene)boranes". Z. Anorg. Allg. Chem. 630: 508–518. doi:10.1002/zaac.200300396.
Curran, D. P., Solovyev, A., Makhlouf Brahmi, M., Fensterbank, L., Malacria, M. and Lacôte, E. (2011), Synthesis and Reactions of N-Heterocyclic Carbene Boranes. Angewandte Chemie International Edition, 50: 10294–10317. எஆசு:10.1002/anie.201102717
Yuzhong Wang, Brandon Quillian, Pingrong Wei, Chaitanya S. Wannere, Yaoming Xie, R. Bruce King, Henry F. Schaefer, III, Paul v. R. Schleyer, and Gregory H. Robinson (2007). "A Stable Neutral Diborene Containing a B=B Double Bond". J. Am. Chem. Soc. 129 (41): 12412–12413. doi:10.1021/ja075932i.

inist.fr

cat.inist.fr

Nicolaou, K.C.; Sarabia, F.; Ninkovic, S.; Finlay, M.R.V.; Boddy, C.N.C. (1998). "Probing The Ring Size Of Epothilones: Total Synthesis Of 14-, 15-, 17-, And 18 Epothilones A". Angewandte Chemie International Edition in English 37 (1–2): 81–84. doi:10.1002/(sici)1521-3773(19980202)37:1/2<81::aid-anie81>3.0.co;2-c. http://cat.inist.fr/?aModele=afficheN&cpsidt=10349604. பார்த்த நாள்: 2008-03-02.

iupac.org

Batey Robert A., Quach Tan D., Shen Ming, Thadani Avinash N., Smil David V., Li Sze-Wan, MacKay D. Bruce (2002). "Organoboron compounds as mild nucleophiles in Lewis acid- and transition metal-catalyzed C–C bond-forming reactions" (PDF). Pure Appl. Chem. 74 (1): 43–55. doi:10.1351/pac200274010043. http://www.iupac.org/publications/pac/2002/pdf/7401x0043.pdf.