485321-76-4

Upstream product

• 76-83-5 trityl chloride 
• 527758-12-9 dimethyl (S)-malate trityl ether 
• 485321-75-3 (S)-2-Trityloxy-succinic acid diethyl ester 

Downstream Products

• 527758-24-3 Methanesulfonic acid (S)-4-methanesulfonyloxy-2-trityloxy-butyl ester 
• 485321-78-6 methanesulfonic acid 4-(tert-butyl-diphenyl-silanyloxy)-2-trityloxy-butyl ester 
• 678172-34-4 (S)-1-(Benzhydrylidene-amino)-3-trityloxy-cyclopentanecarboxylic acid ethyl ester 
• 527758-14-1 1,4-diiodo-2(S)-trityl-oxybutane 
• 485321-77-5 4-(tert-butyl-diphenyl-silanyloxy)-2-trityloxy-butan-1-ol 

Relevant academic research and scientific papers

α-cycloPNA: 1-Aminocylopentane-1-carboxylic acid-derived peptide nucleic acid

All four diastereoisomers of 3-thymine-1-( tbutoxycarbonyl)aminocyclopentane-1-carboxylic acid have been synthesised from (S)-dimethyl malate and thymine monomer 12 has been incorporated into an α-cycloPNA oligomer.

Synthesis of the four diastereoisomers of 3-thymine-1-(tbutoxycarbonyl)aminocyclopentane-1-carboxylic acid

Synthetic routes to all four diastereoisomers of 3-thymine-1-(tbutoxycarbonyl)aminocyclopentane-1-carboxylic acid have been developed starting from the commercially available (S)-dimethyl malate. The key step in the synthesis involves dialkylat

First total synthesis and determination of the absolute configuration of strictifolione, a new 6-(ω-phenylalkenyl)-5,6-dihydro-α-pyrone, isolated from Cryptocarya strictifolia

Starting from (S)-malic acid and (S)-glycidol, the first total synthesis of strictifolione, a new 6-(ω-phenylalkenyl)-5,6-dihydro-α-pyrone isolated from Cryptocarya strictifolia, was accomplished, which confirmed its structure including the absolute confi