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Pure Appl. Chem., 2001, Vol. 73, No. 2, pp. 337-341

Chemistry of 1,2-allenyl/propargyl metal species. A personal account

Sheng-Ming Ma and Ai-Bin Zhang

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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  • Ardolino Michael J., Eno Meredith S., Morken James P.: Stereocontrol in Palladium-Catalyzed Propargylic Substitutions: Kinetic Resolution to give Enantioenriched 1,5-Enynes and Propargyl Acetates. Adv. Synth. Catal. 2013, 355, 3413. <>
  • Ardolino Michael J., Morken James P.: Construction of 1,5-Enynes by Stereospecific Pd-Catalyzed Allyl–Propargyl Cross-Couplings. J. Am. Chem. Soc. 2012, 134, 8770. <>
  • Fandrick Daniel R., Saha Jaideep, Fandrick Keith R., Sanyal Sanjit, Ogikubo Junichi, Lee Heewon, Roschangar Frank, Song Jinhua J., Senanayake Chris H.: Zinc-Catalyzed Allenylations of Aldehydes and Ketones. Org Lett 2011, 13, 5616. <>
  • Ma Sheng-Ming, Zhang Ai-Bin: ChemInform Abstract: Chemistry of 1,2-Allenyl/Propargyl Metal Species. A Personal Account. ChemInform 2010, 32, no. <>
  • Schneider Uwe, Sugiura Masaharu, Kobayashi Shū: Highly Selective Preparation of Allenic and Homopropargylic Hydrazides through Regiospecific Addition of Propargyltrichlorosilane and Allenyltrichlorosilane to Various Types ofN-Acylhydrazones. Adv Synth Catal 2006, 348, 323. <>