184777-79-5

Downstream Products

• 184777-88-6 3-(2-Benzyloxy-3,5-dibromo-4-methoxy-phenyl)-2-[(Z)-hydroxyimino]-N-(3-methoxy-propyl)-propionamide 
• 155697-03-3 3-(3,5-Dibromo-2-hydroxy-4-methoxy-phenyl)-2-[(Z)-hydroxyimino]-N-(3-methoxy-propyl)-propionamide 
• 206991-24-4 {2-[4-(3-{3-(2-Benzyloxy-3,5-dibromo-4-methoxy-phenyl)-2-[(Z)-hydroxyimino]-propionylamino}-propoxy)-3,5-dibromo-phenyl]-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester 
• 206991-20-0 {2-[4-(3-{3-(2-Benzyloxy-3,5-dibromo-4-methoxy-phenyl)-2-[(Z)-hydroxyimino]-propionylamino}-propoxy)-3,5-dibromo-phenyl]-ethyl}-carbamic acid tert-butyl ester 
• 87580-06-1 benzyl 2-benzyloxyimino-3-(2-benzyloxy-3,5-dibromo-4-methoxyphenyl)propionate 

Relevant academic research and scientific papers

Oxidative cyclisation of o-phenolic oxime-acid derivatives using phenyliodonium diacetate: Synthesis of spiroisoxazoline derivatives

An efficient formation of spiroisoxazoline ring system by intramolecular oxidative cyclisation of o-phenolic oxime-esters and oxime-amides using phenyliodonium diacetate (PIDA) is described. The intramolecular oxidative cyclisation of various o-phenolic o

TOTAL SYNTHESES OF (+/-)-AEROTHIONIN AND (+/-)-HOMOAEROTHIONIN

Both aerothionin and homoaerothionin, the novel metabolites of the sponges Aplysina aerophoba, A. fistularis and Verongia thiona, have been synthesized in racemic form.