Simple Preparation of N-Protected Chiral β-Amino Alkyl Thiols from Corresponding Iodides Employing Sodium Trithiocarbonate

Chilakapati Madhu Peptide Research Laboratory, Department of Studies in Chemistry, Central College Campus, Bangalore University, Bangalore, India

H. P. Hemantha Peptide Research Laboratory, Department of Studies in Chemistry, Central College Campus, Bangalore University, Bangalore, India

T. M. Vishwanatha Peptide Research Laboratory, Department of Studies in Chemistry, Central College Campus, Bangalore University, Bangalore, India

V. V. Sureshbabu Peptide Research Laboratory, Department of Studies in Chemistry, Central College Campus, Bangalore University, Bangalore, IndiaCorrespondence[email protected] ; [email protected] ; [email protected]

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Damiano Tanini, Giulia Barchielli, Francesca Benelli, Alessandro Degl’Innocenti & Antonella Capperucci. (2015) Aziridines Ring Opening by Silyl Chalcogenides: a Stereoselective Access to Polyfunctionalized Molecules as Precursor of Sulfurated and Selenated Heterocycles. Phosphorus, Sulfur, and Silicon and the Related Elements 190:8, pages 1265-1270.
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M. Isabel Cabaço, Marcel Besnard, Fabián Vaca Chávez, Noël Pinaud, Pedro J. Sebastião, João A. P. Coutinho & Yann Danten. (2014) Understanding chemical reactions of CO2 and its isoelectronic molecules with 1-butyl-3-methylimidazolium acetate by changing the nature of the cation: The case of CS2 in 1-butyl-1-methylpyrrolidinium acetate studied by NMR spectroscopy and density functional theory calculations. The Journal of Chemical Physics 140:24.
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Chilakapati Madhu, H. P. Hemantha, T. M. Vishwanatha & V. V. Sureshbabu. (2013) ChemInform Abstract: Simple Preparation of N‐Protected Chiral α‐Amino Alkyl Thiols from Corresponding Iodides Employing Sodium Trithiocarbonate.. ChemInform 44:18.
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Simple Preparation of N-Protected Chiral β-Amino Alkyl Thiols from Corresponding Iodides Employing Sodium Trithiocarbonate

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Simple Preparation of N-Protected Chiral β-Amino Alkyl Thiols from Corresponding Iodides Employing Sodium Trithiocarbonate

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