Pure and Applied Chemistry

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• Thakur Ashish, Facer Megan E., Louie Janis: Nickel-Catalyzed Cycloaddition of 1,3-Dienes with 3-Azetidinones and 3-Oxetanones. Angew. Chem. 2013, 125, 12383. <http://dx.doi.org/10.1002/ange.201306869>
• Thakur Ashish, Facer Megan E., Louie Janis: Nickel-Catalyzed Cycloaddition of 1,3-Dienes with 3-Azetidinones and 3-Oxetanones. Angew. Chem. Int. Ed. 2013, 52, 12161. <http://dx.doi.org/10.1002/anie.201306869>
• Cornella Josep, Gómez-Bengoa Enrique, Martin Ruben: Combined Experimental and Theoretical Study on the Reductive Cleavage of Inert C–O Bonds with Silanes: Ruling out a Classical Ni(0)/Ni(II) Catalytic Couple and Evidence for Ni(I) Intermediates. J. Am. Chem. Soc. 2013, 135, 1997. <http://dx.doi.org/10.1021/ja311940s>
• Matsubara Ryosuke, Jamison Timothy F.: Nickel-Catalyzed Allylic Substitution of Simple Alkenes. Chem —Asian J 2011, 6, 1860. <http://dx.doi.org/10.1002/asia.201000875>
• Ohashi Masato, Taniguchi Tomoaki, Ogoshi Sensuke: Nickel-Catalyzed Formation of Cyclopentenone Derivatives via the Unique Cycloaddition of α,β-Unsaturated Phenyl Esters with Alkynes. J. Am. Chem. Soc. 2011, 133, 14900. <http://dx.doi.org/10.1021/ja2059999>
• Cho Hee Yeon, Yu Zhiyong, Morken James P.: Stereoselective Borylative Ketone-Diene Coupling. Org Lett 2011, 13, 5267. <http://dx.doi.org/10.1021/ol202138v>
• Reichard Holly A., Micalizio Glenn C.: Metallacycle-mediated cross-coupling with substituted and electronically unactivated alkenes. Chem Sci 2011, 2, 573. <http://dx.doi.org/10.1039/c0sc00394h>
• Hatakeyama Takuji, Ishizuka Kentaro, Nakamura Masaharu: Cross-Coupling Reactions Catalyzed by Iron Group Metals and N-Heterocyclic Carbenes via Nonconventional Reaction Mechanisms. J Syn Org Chem Jpn 2011, 69, 1282. <http://dx.doi.org/10.5059/yukigoseikyokaishi.69.1282>
• Barlan Allan U., Micalizio Glenn C.: The regio- and stereochemical course of reductive cross-coupling reactions between 1,3-disubstituted allenes and vinylsilanes: synthesis of (Z)-dienes. Tetrahedron 2010, 66, 4775. <http://dx.doi.org/10.1016/j.tet.2010.02.062>
• Matsubara Ryosuke, Jamison Timothy F.: Nickel-Catalyzed Allylic Substitution of Simple Alkenes. J Am Chem Soc 2010, 132, 6880. <http://dx.doi.org/10.1021/ja101186p>
• Liu Peng, McCarren Patrick, Cheong Paul Ha-Yeon, Jamison Timothy F., Houk K. N.: Origins of Regioselectivity and Alkene-Directing Effects in Nickel-Catalyzed Reductive Couplings of Alkynes and Aldehydes. J Am Chem Soc 2010, 132, 2050. <http://dx.doi.org/10.1021/ja909562y>
• Takahashi Masayuki, Micalizio Glenn C.: Concerning the potential reversibility of carbometalation in alkoxide-directed Ti(Oi-Pr)4-mediated reductive cross-coupling of homoallylic alcohols with aromatic imines. Chem Commun 2010, 46, 3336. <http://dx.doi.org/10.1039/b927430h>
• Ho Chun-Yu, Chan Chun-Wa, Wo Siu-Kwan, Zuo Zhong, Chan Lai-Ying: Nitrile assisted, Brønsted acid catalyzed regio and stereoselective diarylphosphonylation of allyl silyl ethers. Org Biomol Chem 2010, 8, 3480. <http://dx.doi.org/10.1039/c001660h>
• Kerrigan Michael H., Jeon Sang-Jin, Chen Young K., Salvi Luca, Carroll Patrick J., Walsh Patrick J.: One-Pot Multicomponent Coupling Methods for the Synthesis of Diastereo- and Enantioenriched (Z)-Trisubstituted Allylic Alcohols. J Am Chem Soc 2009, 131, 8434. <http://dx.doi.org/10.1021/ja809821x>
• McCarren P. R., Liu Peng, Cheong Paul Ha-Yeon, Jamison Timothy F., Houk K. N.: Mechanism and Transition-State Structures for Nickel-Catalyzed Reductive Alkyne−Aldehyde Coupling Reactions. J Am Chem Soc 2009, 131, 6654. <http://dx.doi.org/10.1021/ja900701g>
• Hatakeyama Takuji, Hashimoto Sigma, Ishizuka Kentaro, Nakamura Masaharu: Highly Selective Biaryl Cross-Coupling Reactions between Aryl Halides and Aryl Grignard Reagents: A New Catalyst Combination of N-Heterocyclic Carbenes and Iron, Cobalt, and Nickel Fluorides. J Am Chem Soc 2009, 131, 11949. <http://dx.doi.org/10.1021/ja9039289>
• Ng Sze-Sze, Ho Chun-Yu, Schleicher Kristin D., Jamison Timothy F.: ChemInform Abstract: Nickel-Catalyzed Coupling Reactions of Alkenes. ChemInform 2008, 39. <http://dx.doi.org/10.1002/chin.200843248>