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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 39, 2009 - Issue 5
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Original Articles

Alkali Salt of L-Proline as an Efficient and Practical Catalyst for the Cyanosilylation of a Wide Variety of Carbonyl Compounds Under Solvent-Free Conditions

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Pages 775-791 | Received 06 May 2008, Published online: 29 Jan 2009

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Murugan Kumaresan, Vijayakumar Karthika, Karuppaiah Selvakumar & Ponnusamy Sami. (2019) Green synthesis of naphtho[2,3-f]quinolin-13-one and naphtho[2,3-a]acridin-1(2H)-one derivatives catalyzed by heteropoly acid supported montmorillonite K-10 clay. Synthetic Communications 49:21, pages 2856-2868.
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Wen-Biao Wu, Xing-Ping Zeng & Jian Zhou. (2020) Carbonyl-Stabilized Phosphorus Ylide as an Organocatalyst for Cyanosilylation Reactions Using TMSCN. The Journal of Organic Chemistry 85:22, pages 14342-14350.
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Richard C. LarockRichard C. Larock & Cristiano Raminelli. 2018. Comprehensive Organic Transformations. Comprehensive Organic Transformations 1 97 .
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Jason R. HudlickyLukas WernerVladislav SemakRazvan SimionescuTomas Hudlicky. (2011) Dauben–Michno oxidative transposition of allylic cyanohydrins — Enantiomeric switch of (–)-carvone to (+)-carvone*Based on the 2010 Bader Award Lecture.. Canadian Journal of Chemistry 89:5, pages 535-543.
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Girijesh K. Verma, Keshav Raghuvanshi, Rajiv K. Verma, Pratibha Dwivedi & M.S. Singh. (2011) An efficient one-pot solvent-free synthesis and photophysical properties of 9-aryl/alkyl-octahydroxanthene-1,8-diones. Tetrahedron 67:20, pages 3698-3704.
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Linhai Jing, Jiangtao Wei, Li Zhou, Zhiyong Huang, Zhengkai Li & Xiangge Zhou. (2010) Lithium pipecolinate as a facile and efficient ligand for copper-catalyzed hydroxylation of aryl halides in water. Chemical Communications 46:26, pages 4767.
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Zhi‐Liang Shen & Shun‐Jun Ji. (2009) ChemInform Abstract: Alkali Salt of L‐Proline as an Efficient and Practical Catalyst for the Cyanosilylation of a Wide Variety of Carbonyl Compounds under Solvent‐Free Conditions.. ChemInform 40:32.
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