936564-33-9

Upstream product

• 501-53-1 benzyl chloroformate 
• 56620-28-1 (5S)-8-methyl-8-azabicyclo[3.2.1]octan-2-one 

Downstream Products

• 936564-35-1 (1R,5S)-N-benzyloxycarbonyl-2-methoxy-8-azabicyclo[3.2.1]oct-2-ene 
• 1234804-88-6 (2S,5S)-benzyloxycarbonyl-2-(2-(tert-butyldiphenylsilyloxy)ethyl)-5-(2-(2,6-dioxocyclohexyl)ethyl)pyrrolidine 
• 1234804-87-5 (2S,5R)-benzyloxycarbonyl-2-(2-(tert-butyldiphenylsilyloxy)ethyl)-5-(2-oxoethyl)pyrrolidine 
• 1234804-86-4 C₃₃H₄₁NO₄Si 
• 1234804-85-3 (2S,5R)-benzyloxycarbonyl-2-(2-(tert-butyldiphenylsilyloxy)ethyl)-5-formylpyrrolidine 
• 1234804-84-2 (2R,5S)-1-benzyloxycarbonyl-5-(2-(tert-butyldiphenylsilyloxy)ethyl)-2-(methoxycarbonyl)pyrrolidine 
• 1234804-82-0 (2R,5S)-1-benzyloxycarbonyl-2-methoxycarbonyl-5-(2-hydroxyethyl)pyrrolidine 
• 1234804-89-7 (1S,3aS)-1-(2-(tert-butyldiphenylsilyloxy)ethyl)-1,2,3,3a,4,5,8,9-octahydropyrrolo-[1,2-a]quinolin-6(7H)-one 
• 936564-39-5 (2R,5S)-N-benzyloxycarbonyl-2-methoxycarbonyl-5-(2,2-dimethoxyethyl)-pyrrolidine 
• 936564-37-3 (2R,5S)-N-benzyloxycarbonyl-2-methoxycarbonyl-5-(2-oxoethyl)-pyrrolidine 

Relevant academic research and scientific papers

Enantioselective syntheses of both enantiomers of cis-pyrrolidine 225H

The efficient and expeditious syntheses of both enantiomers of the amphibian alkaloid cis-225H have been achieved. Utilizing a common cis-2,5-disubstituted pyrrolidine building block derived from (+)-2-tropinone, the enantioselective syntheses have establ

General strategy for the construction of enantiopure pyrrolidine-based alkaloids. Total synthesis of (-)-monomorine

(Chemical Equation Presented) An enantiopure cis-2,5-disubstituted pyrrolidine building block was prepared from cocaine. The synthetic utility of this compound as a chiral building block was demonstrated by a short and efficient synthesis of the pyrrolidi