The Choice of Tools for Implementing Multistage Transformations. SPOS for Beginners
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-50015-7_2
Reference14 articles.
1. O’Donnell MJ, Zhou C, Scott WL (1996) Solid-phase unnatural peptide synthesis (UPS). J Am Chem Soc 118:6070–6071. doi: 10.1021/ja9601245
2. (a) Scott WL, Zhou C, Fang Z, O’Donnell MJ (1997) The solid phase synthesis of α,α-disubstituted unnatural amino acids and peptides (di-UPS). Tetrahedron Lett 38: 3695–3698. doi: 10.1016/S0040-4039(97)00715-6 . (b) Alsina J, Scott WL, O’Donnell MJ (2005) Solid-phase synthesis of α-substituted proline hydantoins and analogs. Tetrahedron Lett 46: 3131–3135. doi: 10.1016/j.tetlet.2005.01.163
3. Scott WL, O’Donnel MJ (2009) Distributed drug discovery, part 1: linking academics and combinatorial chemistry to find drugs for developing world diseases. J Comb Chem 11:3–13. doi: 10.1021/cc800183m
4. Scott WL, Alsina J, Audu CO, Dage JL, Babaev EV, Cook L, Dage JL, Goodwin LA, Martynow JG, Matosiuk D, Royo M, Smith JG, Strong AT, Wickizer K, Woerly EM, Zhou Z, O’Donnell MJ (2009) Distributed drug discovery, part 2: global rehearsal of alkylating agents for the synthesis of resin-bound unnatural amino acids and virtual D3 catalog construction. J Comb Chem 11:14–33. doi: 10.1021/cc800184v
5. Houghten RA (1985) General method for the rapid solid-phase synthesis of large numbers of peptides: specificity of antigen-antibody interaction at the level of individual amino acids. Proc Nat Acad Sci 82(15):5131–5135. doi: 10.1073/pnas.82.15.5131
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