Boron Attacks Electropositive element pressed into action as nucleophilic boryllithium Bethany Halford Chemical & Engineering News October 9, 2006 Volume 84, Number 41 p. 11 Link （页面存档备份，存于互联网档案馆）
Bent, Henry E.; Dorfman, Maurice. PENTAVALENT BORON. Journal of the American Chemical Society (American Chemical Society (ACS)). 1932, 54 (5): 2132–2133. ISSN 0002-7863. doi:10.1021/ja01344a511.
Bent, Henry E.; Dorfman, Maurice. The Conductance of Non-aqueous Solutions. I. Sodium Triphenylboron and Disodium Tri-α-naphthylboron in Diethyl Ether. Journal of the American Chemical Society (American Chemical Society (ACS)). 1935, 57 (10): 1924–1927. ISSN 0002-7863. doi:10.1021/ja01313a051.
Conversion of Arylboronic Acids into Potassium Aryltrifluoroborates: Convenient Precursors of Arylboron Difluoride Lewis Acids E. Vedejs, R. W. Chapman, S. C. Fields, S. Lin, M. R. Schrimpf J. Org. Chem.1995; 60(10); 3020–3027. doi:10.1021/jo00115a016
Organotrifluoroborates and Monocoordinated Palladium Complexes as Catalysts—A Perfect Combination for Suzuki–Miyaura Coupling Gary A. Molander and Belgin Canturk Angew. Chem. Int. Ed.2009, 48, 9240 – 9261doi:10.1002/anie.200904306
Boryllithium: Isolation, Characterization, and Reactivity as a Boryl Anion Yasutomo Segawa, Makoto Yamashita, Kyoko NozakiScience 6 October 2006:
Vol. 314. no. 5796, pp. 113 – 115 doi:10.1126/science.1131914
Reactions at the Boron-Carbon Double Bond of Methyl(methylidene)boranes
Peter Paetzold, Ulli Englert, Rudolf Finger, Thomas Schmitz, Alexander Tapper, and Ralf Ziembinski Z. Anorg. Allg. Chem. 2004, 630, 508–518 doi:10.1002/zaac.200300396
A Stable Neutral Diborene Containing a BdB Double Bond 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 doi:10.1021/ja075932i
Organoboron compounds as mild nucleophiles in Lewis acid- and transition metal-catalyzed
C–C bond-forming reactions Robert A. Batey, Tan D. Quach, Ming Shen, Avinash N. Thadani, David V. Smil, Sze-Wan Li, and D. Bruce MacKay Pure Appl. Chem., Vol. 74, No. 1, pp. 43–55, 2002. http://www.iupac.org/publications/pac/2002/pdf/7401x0043.pdf （页面存档备份，存于互联网档案馆）
Organoboron compounds as mild nucleophiles in Lewis acid- and transition metal-catalyzed
C–C bond-forming reactions Robert A. Batey, Tan D. Quach, Ming Shen, Avinash N. Thadani, David V. Smil, Sze-Wan Li, and D. Bruce MacKay Pure Appl. Chem., Vol. 74, No. 1, pp. 43–55, 2002. http://www.iupac.org/publications/pac/2002/pdf/7401x0043.pdf （页面存档备份，存于互联网档案馆）
Boron Attacks Electropositive element pressed into action as nucleophilic boryllithium Bethany Halford Chemical & Engineering News October 9, 2006 Volume 84, Number 41 p. 11 Link （页面存档备份，存于互联网档案馆）
Bent, Henry E.; Dorfman, Maurice. PENTAVALENT BORON. Journal of the American Chemical Society (American Chemical Society (ACS)). 1932, 54 (5): 2132–2133. ISSN 0002-7863. doi:10.1021/ja01344a511.
Bent, Henry E.; Dorfman, Maurice. The Conductance of Non-aqueous Solutions. I. Sodium Triphenylboron and Disodium Tri-α-naphthylboron in Diethyl Ether. Journal of the American Chemical Society (American Chemical Society (ACS)). 1935, 57 (10): 1924–1927. ISSN 0002-7863. doi:10.1021/ja01313a051.
