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Joule, J. A., Science of Synthesis, (2001) 10, 445..
From N-[o-(Acylmethyl)-, N-[o-(Cyanomethyl)-, N-[o-(Alkoxycarbonylmethyl)-, or N-[o-(Phenylsulfonylmethyl)aryl]amides
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Science of Synthesis
Augustine, John Kallikat; Atta, Rajendra Nath; Ramappa, Balakrishna Kolathur; Boodappa, Chandrakantha, Synlett 2009, 3378-3382.
Propylphosphonic Anhydride (T3P®): A Remarkably Efficient Reagent for the One-Pot Transformation of Aromatic, Heteroaromatic, and Aliphatic Aldehydes to Nitriles
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Synlett
[DOI: 10.1055/s-0029-1218388]
Yan, G.; Zhang, Y.; Wang, Jianbo, Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 2, 542..
Cyanation through Direct C—H Bond Activation
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Science of Synthesis
Vishwanatha, T. M.; Panguluri, Nageswara Rao; Sureshbabu, Vommina V., Synthesis 2013, 45, 1569-1601.
Propanephosphonic Acid Anhydride (T3P?) - A Benign Reagent for Diverse Applications Inclusive of Large-Scale Synthesis
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Synthesis
[DOI: 10.1055/s-0033-1338989]