9 research outputs found
One-Pot Synthesis of Polynuclear Indole Derivatives by Friedel–Crafts Alkylation of γ-Hydroxybutyrolactams
No full textThe Friedel–Crafts reaction of novel 3,5-diarylsubstituted 5-hydroxy-1,5-dihydro-2H-pyrrol-2-ones was used for low cost, one-pot preparation of polycyclic indole derivatives structurally similar to Ergot alkaloids
A Simple Route to Polysubstituted Indoles Exploiting Azide Induced Furan Ring Opening
No full textA straightforward, efficient indole
synthesis based on thermolysis of 2-(2-azidobenzyl)furans
with attack of the formed nitrene moiety onto the <i>ipso</i> position of furan ring has been developed. The cyclization is accompanied
by furan ring opening and affords indoles with a 2-acylvinyl substituent
suitable for further modifications
Lytic activity of the staphylolytic Twort phage endolysin CHAP domain is enhanced by the SH3b cell wall binding domain
No full textA simple synthesis of benzofurans by acid-catalyzed domino reaction of salicyl alcohols with N -tosylfurfurylamine
No full textStaphylococcal Phage 2638A endolysin is lytic for Staphylococcus aureus and harbors an inter-lytic-domain secondary translational start site
No full textFuran ring opening–pyrrole ring closure: a new synthetic route to aryl(heteroaryl)-annulated pyrrolo[1,2-a][1,4]diazepines
No full text
