Molecular Iodine-Catalyzed Facile Procedure for N-Boc Protection of Amines

Related Content

• Catalyst-Free Chemoselective N-tert-Butyloxycarbonylation of Amines in WaterOrganic Letters

  • Catalyst-Free Chemoselective N-tert-Butyloxycarbonylation of Amines in Water

    Sunay V. Chankeshwara and Asit K. Chakraborti
    Organic Letters 2006 8 (15), pp 3259–3262

    Abstract: Catalyst-free N-tert-butyloxycarbonylation of amines in water is reported. The N-t-Boc derivatives were formed chemoselectively without any isocyanate, urea, N,N-di-t-Boc, and O/S-t-Boc as side products. Chiral amines, esters of α-amino acids, and β-amino ...

    Abstract | Full Text HTML | Hi-Res PDF
• Mitsunobu and Related Reactions: Advances and ApplicationsChemical Reviews

  • Mitsunobu and Related Reactions: Advances and Applications

    K. C. Kumara Swamy, N. N. Bhuvan Kumar, E. Balaraman and K. V. P. Pavan Kumar
    Chemical Reviews 2009 109 (6), pp 2551–2651
    Abstract | Full Text HTML | PDF w/ Links | Hi-Res PDF
• Highly Efficient Stereoconservative Amidation and Deamidation of α-Amino AcidsOrganic Letters

  • Highly Efficient Stereoconservative Amidation and Deamidation of α-Amino Acids

    Deepak M. Shendage, Roland Fröhlich, and Günter Haufe
    Organic Letters 2004 6 (21), pp 3675–3678

    Abstract: An overall stereoconservative protection and deprotection method of amino and carboxyl groups is presented. N-Phthaloyl N‘-alkyl secondary amides of α-amino acids can be generated from corresponding N-phthaloyl amino acids by coupling reaction of N-...

    Abstract | Full Text HTML | Hi-Res PDF

Other ACS content by these authors:

• Ravi Varala
• Sreelatha Nuvula
• Srinivas R. Adapa