Literature DB >> 8407109

Synthesis and stability of 3-nitro-2-pyridinesulfenyl chloride (NpysCl).

K C Pugh1, L Gera, J M Stewart.   

Abstract

3-Nitro-2-pyridinesulfenyl chloride (NpysCl) is the starting material for the synthesis of N-, O- and S-Npys-protected amino acids. Two efficient, novel synthetic routes to NpysCl are described. The stability of NpysCl was determined in a variety of solvents, with and without base, to determine the most suitable solvent and base for the synthesis of N-Npys amino acids. The syntheses of Npys-Ala and Boc-Lys(Npys) tert-butylammonium salt are also described.

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Year:  1993        PMID: 8407109     DOI: 10.1111/j.1399-3011.1993.tb00492.x

Source DB:  PubMed          Journal:  Int J Pept Protein Res        ISSN: 0367-8377


  2 in total

1.  Studies on chymotrypsin-like catalysis by synthetic peptides.

Authors:  M J Corey; E Hallakova; K Pugh; J M Stewart
Journal:  Appl Biochem Biotechnol       Date:  1994 May-Jun       Impact factor: 2.926

2.  Synthesis and Biological Activity of Unsymmetrical Monoterpenylhetaryl Disulfides.

Authors:  Denis V Sudarikov; Yulia V Gyrdymova; Alexander V Borisov; Julia M Lukiyanova; Roman V Rumyantcev; Oksana G Shevchenko; Diana R Baidamshina; Nargiza D Zakarova; Airat R Kayumov; Ekaterina O Sinegubova; Alexandrina S Volobueva; Vladimir V Zarubaev; Svetlana A Rubtsova
Journal:  Molecules       Date:  2022-08-10       Impact factor: 4.927

  2 in total

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