129575-00-4

Upstream product

• 123043-38-9 N-trans-3-(4-cyanophenoxy)-1-glycyl>-L-prolyl-L-isoleucine methyl ester 
• 75-52-5 nitromethane 
• 129574-99-8 N-<1-glycyl>-trans-3-<4-(formylphenoxy)-L-prolyl>-L-isoleucine methyl ester 

Downstream Products

• 129575-01-5 N-<1-glycyl>-trans-3-<4-(1,1-dimethylethyl)dimethylsilyloxy>-2-(nitroethyl)phenoxy-L-prolyl-L-isoleucine methyl ester 
• 129574-98-7 N-oxy>ethyl>-phenoxy>-1-glycyl>-L-prolyl>-L-isoleucine 
• 129575-02-6 N-oxy>ethyl>-phenoxy>-1--L-prolyl-L-isoleucine methyl ester 
• 129575-04-8 N-<1-glycyl>trans-3-<4-<1-<<(1,1-dimethylethyl)dimethylsilyl>oxy>-2-<<(phenylmethoxy)carbonyl>amino>-ethyl>phenoxy>-L-prolyl>-L-isoleucine 
• 129575-03-7 N-<1-glycyl>trans-3-<4-<1-<<(1,1-dimethylethyl)dimethylsilyl>oxy>-2-<<(phenylmethoxy)carbonyl>amino>ethyl>phenoxy>-L-prolyl>-L-isoleucine methyl ester 

Relevant academic research and scientific papers

Studies Directed Toward the Total Synthesis of 14-Membered Cyclopeptide Alkaloids: Synthesis of a Linear Precursor to Nummularine-F

Investigations leading to the synthesis of a linear precursor (2) to the 14-membered cyclopeptide alkaloid, nummularine-F, are described.The Ugi four-component condensation reaction was utilized to prepare the key intermediate (3) which, under mild condit