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Pure Appl. Chem., 2007, Vol. 79, No. 2, pp. 261-267

http://dx.doi.org/10.1351/pac200779020261

Control of regio- and stereoselectivity in electrophilic addition reactions of allenes

Shengming Ma

Laboratory of Molecular Recognition and Synthesis, Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang 310027 and State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, P. R. China

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  • Laali Kenneth K., Nandi Ganesh C., Borosky Gabriela L., Kumar G. G. K. S. Narayana: Electrophilic Addition of Propargylic Cations to Allenes: Formation of Crowded Chloro- and Azido-Enynes by Trapping of the Resulting Allylic Cations with TMSX (X = Cl, N3 ): A Synthetic and Computational Study. Eur. J. Org. Chem. 2013, 2013, 5455. <http://dx.doi.org/10.1002/ejoc.201300553>
  • Wang Minyan, Fu Chunling, Ma Shengming: Cleavage of oxygen–sulfur double bonds and carbon–sulfur bonds: unusual highly selective electrophilic addition of allenylic sulfoxides. Chem. Sci. 2013, 4, 1016. <http://dx.doi.org/10.1039/c2sc21920d>
  • Yu Shichao, Ma  Shengming: Allene in katalytischer asymmetrischer Synthese und Naturstoffsynthese. angew chemie 2012, 124, 3128. <http://dx.doi.org/10.1002/ange.201101460>
  • Yu Shichao, Ma Shengming: Allenes in Catalytic Asymmetric Synthesis and Natural Product Syntheses. Angew Chem Int E 2012, 51, 3074. <http://dx.doi.org/10.1002/anie.201101460>
  • Meng Bo, Ma Shengming: Carbon–Carbon Bond Formation via the Electrophilic Addition of Carbocations to Allenes. Z Org Lett 2012, 120514143752009. <http://dx.doi.org/10.1021/ol3006985>
  • Liu Cong-Rong, Wang Ting-Ting, Qi Qing-Biao, Tian Shi-Kai: Ferric chloride-catalyzed C–N bond cleavage for the cyclization of arylallenes leading to polysubstituted indenes. Chem. Commun. 2012, 48, 10913. <http://dx.doi.org/10.1039/c2cc36048a>
  • He Guangke, Yu Yihua, Fu Chunling, Ma Shengming: Highly Selective Synthesis of [(Z)-3-Chloro-2-(phenylselanyl)-1-alkenyl]phosphonates and 2-Ethoxy-4-(phenylselanyl)-2,5-dihydro-1,2-oxaphosphole 2-Oxides by Electrophilic Reaction of 1,2-Alkadienylphosphonates with PhSeCl. Eur J Org 2010, 2010, 101. <http://dx.doi.org/10.1002/ejoc.200900913>
  • Ruano José Luis García, Marcos Vanesa, Alemán José: Complete Regio- and Stereoselectivity Control in the Halohydroxylation of Non-activated Allenes Mediated by a Remote Sulfinyl Group. Angew Chem 2009, 121, 3201. <http://dx.doi.org/10.1002/ange.200900448>
  • Ruano José Luis García, Marcos Vanesa, Alemán José: Complete Regio- and Stereoselectivity Control in the Halohydroxylation of Non-activated Allenes Mediated by a Remote Sulfinyl Group. Angew Chem Int Ed 2009, 48, 3155. <http://dx.doi.org/10.1002/anie.200900448>
  • Lian Xiongdong, Ma Shengming: An Efficient Approach to Substituted 1,5,7,8,9-Pentahydrocyclopenta[h]-2-Benzopyran-3-one Derivatives by a Palladium-Catalyzed Tandem Reaction of 2,7-Alkadiynylic Carbonates with 2,3-Allenoic Acids. Angew Chem 2008, 120, 8379. <http://dx.doi.org/10.1002/ange.200803424>
  • Lian Xiongdong, Ma Shengming: An Efficient Approach to Substituted 1,5,7,8,9-Pentahydrocyclopenta[h]-2-Benzopyran-3-one Derivatives by a Palladium-Catalyzed Tandem Reaction of 2,7-Alkadiynylic Carbonates with 2,3-Allenoic Acids. Angew Chem Int Ed 2008, 47, 8255. <http://dx.doi.org/10.1002/anie.200803424>
  • Ma Shengming: Control of Regio- and Stereoselectivity in Electrophilic Addition Reactions of Allenes. ChemInform 2007, 38. <http://dx.doi.org/10.1002/chin.200729244>