## Abstract For Abstract see ChemInform Abstract in Full Text.
An efficient protocol for the solid-phase synthesis of glycopeptides under microwave irradiation
โ Scribed by Garcia-Martin, Fayna; Hinou, Hiroshi; Matsushita, Takahiko; Hayakawa, Shun; Nishimura, Shin-Ichiro
- Book ID
- 118152872
- Publisher
- Royal Society of Chemistry
- Year
- 2012
- Tongue
- English
- Weight
- 763 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1477-0520
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
7-Chloromethyl-6-nitro-5H-thiazolo[3,2-a]pyrimidin-5-one (2) is obtained by cyclocondensation of 2aminothiazole with ethyl 4-chloroacetoacetate. This product was shown to react with various nitronate or malonate anions under microwave irradiation to give potentially bioactive 6-nitro-5H-thiazolo[3,2
2,3-Dihydro-1H-1,5-benzodiazepines have been synthesized in solvent-free conditions from o-phenylenediamines and ketones in the presence of a catalytic amount of acetic acid, under microwave irradiation. This method is a very easy, rapid and high yielding reaction for the synthesis of 1,5-benzodiaze