873869-01-3

Upstream product

• 162107-48-4 tert-butyl (R)-4-ethynyl-2,2-dimethyloxazolidine-3-carboxylate 

Downstream Products

• 253801-58-0 4-(4-methoxy-7-phenoxy-benzofuran-5-yl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 873869-15-9 (R)-Benzyloxycarbonylamino-(4-methoxy-7-phenoxy-benzofuran-5-yl)-acetic acid 
• 873869-10-4 [(R)-2-Hydroxy-1-(4-methoxy-7-phenoxy-benzofuran-5-yl)-ethyl]-carbamic acid benzyl ester 
• 877265-48-0 [(R)-1-(4-Methoxy-7-phenoxy-benzofuran-5-yl)-2-oxo-ethyl]-carbamic acid benzyl ester 
• 877265-05-9 (R)-2-Amino-2-(4-methoxy-7-phenoxy-benzofuran-5-yl)-ethanol 

Relevant academic research and scientific papers

Synthesis of arylglycines via the D?tz benzannulation reaction

Arylglycines are biologically active α-amino acids. Our approach toward the synthesis of arylglycines features the Do?tz benzannulation reaction between a variety of Fischer chromium carbene complexes 3 and alkyne 4. This leads to the formation of protect

Diaryl ethers using fischer chromium carbene mediated benzannulation

(formula presented) The biological relevance and irresistible synthetic challenge of compounds containing the diaryl ether linkage encourages the development of new methodologies targeted toward this structural subunit. The syntheses of diaryl ethers 2 us