5.07 - N-Heterosubstituted Amides
-
Add time:09/06/2019 Source:sciencedirect.com
This chapter provides a comprehensive survey of the literature over the period 1995–2003 of the chemical transformations involved in the synthesis of N-heterosubstituted amides, that is, compounds that contain at least one carbon atom that has one doubly bonded oxygen atom and one singly bonded nitrogen atom with any other bonded heteroatom attached to it. A wide range of synthetic organic chemistry will be represented detailing methods that involve solution-phase chemistry and solid-supported phase chemistry incorporating both traditional and modern techniques such as the use of microwaves for the synthesis of N-heterosubstituted amides. The chapter is organized in an efficient manner so as to allow all scientists to easily access the information documenting the functional group interconversions required.
We also recommend Trading Suppliers and Manufacturers of N-[(Benzyloxy)carbonyl]-L-serine (pentachlorophenyl) ester (cas 13673-57-9). Pls Click Website Link as below: cas 13673-57-9 suppliers
Prev:Magnetic interaction of iron(II)-iron(III) complexes with carboxylic acid
Next:Synthesis of glycopeptide derivatives containing the 2-acetamido-N-(L-aspart-4-oyl)-2-deoxy-β-D-glucopyranosylamine linkage and having the amino acid sequences 32–34, 33–35,33–37, and 33–38 of bovine ribonuclease) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- The synthesis, and study of the β-elimination reaction, of di- and tri-peptides having a 3-O(2-acetamido-3,4,6-trio-O-acetyl-2-deoxy-β-D-glucopyranosyl)-L-serine residue☆09/08/2019
- Synthesis of glycopeptide derivatives containing the 2-acetamido-N-(L-aspart-4-oyl)-2-deoxy-β-D-glucopyranosylamine linkage and having the amino acid sequences 32–34, 33–35,33–37, and 33–38 of bovine ribonuclease09/07/2019


