691006-74-3

Upstream product

• 874349-35-6 (2S,3R,3aR,4S)-2-[9-(4-Methoxy-benzyloxy)-nonyl]-4-triisopropylsilanyloxy-hexahydro-pyrrolo[1,2-b]isoxazole-3-carboxylic acid ethyl ester 
• 691006-85-6 (2S,3S,3aR,4S)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-2-[9-(4-methoxy-benzyloxy)-nonyl]-hexahydro-pyrrolo[1,2-b]isoxazol-4-ol 
• 691006-73-2 (2S,3S,3aR,4S)-3-Hydroxymethyl-2-[9-(4-methoxy-benzyloxy)-nonyl]-hexahydro-pyrrolo[1,2-b]isoxazol-4-ol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 691006-86-7 thiocarbonic acid O-{3-(tert-butyl-dimethyl-silanyloxymethyl)-2-[9-(4-methoxy-benzyloxy)-nonyl]-hexahydro-pyrrolo[1,2-b]isoxazol-4-yl} ester O-phenyl ester 

Downstream Products

• 874349-38-9 1-tert-butoxycarbonylimino-4-formyl-3-[9-(4-methoxy-benzyloxy)-nonyl]-hexahydro-pyrrolo[1,2-c]pyrimidine-2-carboxylic acid tert-butyl ester 
• 874349-37-8 1-tert-butoxycarbonylimino-3-[9-(4-methoxy-benzyloxy)-nonyl]-hexahydro-pyrrolo[1,2-c]pyrimidine-2,4-dicarboxylic acid 2-tert-butyl ester 
• 691006-78-7 1-tert-butoxycarbonylimino-4-formyl-3-[9-(4-methoxy-benzyloxy)-nonyl]-3,5,6,7-tetrahydro-pyrrolo[1,2-c]pyrimidine-2-carboxylic acid tert-butyl ester 
• 691006-70-9 1-tert-butoxycarbonylimino-4-hydroxymethyl-3-[9-(4-methoxy-benzyloxy)-nonyl]-hexahydro-pyrrolo[1,2-c]pyrimidine-2-carboxylic acid tert-butyl ester 
• 874349-39-0 1-tert-butoxycarbonylimino-3-[9-(4-methoxy-benzyloxy)-nonyl]-3,5,6,7-tetrahydro-pyrrolo[1,2-c]pyrimidine-2,4-dicarboxylic acid 2-tert-butyl ester 
• 691006-76-5 1-tert-butoxycarbonylimino-4-(tert-butyl-dimethyl-silanyloxymethyl)-3-[9-(4-methoxy-benzyloxy)-nonyl]-hexahydro-pyrrolo[1,2-c]pyrimidine-2-carboxylic acid tert-butyl ester 
• 691006-75-4 (tert-butoxycarbonylimino-{2-[1-(tert-butyl-dimethyl-silanyloxymethyl)-2-hydroxy-11-(4-methoxy-benzyloxy)-undecyl]-pyrrolidin-1-yl}-methyl)-carbamic acid tert-butyl ester 
• 691006-87-8 C₅₀H₈₀N₆O₁₂ 
• 874349-36-7 (2S,3S)-1-(tert-Butyl-dimethyl-silanyloxy)-12-(4-methoxy-benzyloxy)-2-(S)-pyrrolidin-2-yl-dodecan-3-ol 

Relevant academic research and scientific papers

Total synthesis of (+)-batzelladine A and (-)-batzelladine D, and identification of their target protein

Asymmetric total synthesis of batzelladine A (1) and batzelladine D (2) has been achieved. Our synthesis of batzelladines features 1) stereoselective construction of the cyclic guanidine system by means of successive 1,3-dipolar cycloaddition reaction and

Enantioselective total synthesis of batzelladine A

One-step formation of an enone from a primary alcohol has been effectively applied in the total synthesis of batzelladine A (1). Successive 1,3-dipolar cycloadditions with a subsequent cyclization were used to form the tricyclic guanidine subunit of this