95245-11-7

Upstream product

• 103-82-2 phenylacetic acid 
• 55628-82-5 1-(Phenylacetyl)imidazole 
• 111-40-0 3-azapentane-1,5-diamine 

Downstream Products

• 757967-03-6 bis-(2-phenylacetylamino-ethyl)-carbamic acid 4-nitro-phenyl ester 
• 757967-06-9 bis-(2-phenylacetylamino-ethyl)-carbamic acid 4-hydroxymethyl-phenyl ester 
• 757967-07-0 carbonic acid 4-[bis-(2-phenylacetylamino-ethyl)-carbamoyloxy]-benzyl ester 4-nitro-phenyl ester 

Relevant academic research and scientific papers

Multi-triggered self-immolative dendritic compounds

Novel self-immolative dendritic compounds which have a plurality of cleavable trigger units and hence can release a chemical moiety at their focal point upon a multi-triggering mechanism are disclosed. The novel self-immolative dendritic compounds are gated by a molecular logic gate, being either an AND or OR logic gate and hence can be beneficially used in a variety of biological, chemical and physical applications. Processes of preparing, compositions containing and methods utilizing the novel dendritic compounds are further disclosed.

Self-immolative dendrimer biodegradability by multi-enzymatic triggering.

New self-immolative dendritic molecules have been designed and synthesized. The dendrons are built with a multi-enzymatic triggering mechanism, which initiates their biodegradation through a self-immolative chain fragmentation to release a reporter group

A SIMPLE METHOD FOR THE DIRECT BIS-ACYLATION THE PRIMARY AMINO GROUPS IN SPERMIDINE AND OTHER LINEAR TRIAMINES

A simple and efficient method for the direct symmetrical bis-acylation of spermidine and other linear triamines using acylimidazoles is described.By this procedure, the siderophore natural product N1,N8-bis(2,3-dihydroxybenzoyl) spermidine was synthesized in an overall yield of 70percent in two steps.