1027388-33-5

Upstream product

• 2216-51-5 (-)-menthol 
• 3740-52-1 2-(2-nitrophenyl)acetic acid 
• 200122-27-6 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-(2-nitrophenyl)acetate 

Downstream Products

• 200122-28-7 (1R,2S,5R)-menthyl 2-(3,4-dihydro)pyrrolidinophenylacetate 
• 200122-30-1 [2-((3aS,6aR)-2,2-Dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyrrol-5-yl)-phenyl]-acetic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 200122-29-8 (1R,2S,5R)-menthyl 2-(3,4-dihydroxy)pyrrolidinophenylacetate 
• 163776-60-1 C₂₅H₃₃NO₄ 
• 163776-52-1 Diazo-[2-((3aS,6aR)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyrrol-5-yl)-phenyl]-acetic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 

Relevant academic research and scientific papers

Synthesis of (-)-Phaitanthrin D and (+)-Dihydropyrroloindoloquinazolinone

The synthesis of (-)-phaitanthrin D and (+)-dihydropyrroloindoloquinazolinone are reported starting from the corresponding especially designed enantiomerically pure pivotal anthranilamide based building blocks using HMDS/ZnCl2 and NaHMDS.

Asymmetric approaches to 1,2-disubstituted mitosenes based on the intramolecular cyclization of diazoesters

A strategy for the asymmetric synthesis of 1,2-disubstituted mitosenes is described. The key reaction is the decomposition of a meso diazoester in the presence of chiral copper(I) catalysts. Cyclization of diazoesters derived from (1R, 2S, 5R)-menthol and