172608-26-3

Upstream product

• 15082-42-5 lithium benzyloxide 
• 184583-22-0 (3aS,8bR)-3-((R)-2-Azido-3-phenyl-propionyl)-4,4-dimethyl-3,3a,4,8b-tetrahydro-indeno[2,1-d]oxazol-2-one 
• 172608-30-9 (3aS,8bR)-4,4-Dimethyl-3-((R)-2-methyl-3-phenyl-propionyl)-3,3a,4,8b-tetrahydro-indeno[2,1-d]oxazol-2-one 

Downstream Products

• 184583-21-9 (3aS,8bR)-3-((S)-2-Bromo-3-phenyl-propionyl)-4,4-dimethyl-3,3a,4,8b-tetrahydro-indeno[2,1-d]oxazol-2-one 
• 184583-22-0 (3aS,8bR)-3-((R)-2-Azido-3-phenyl-propionyl)-4,4-dimethyl-3,3a,4,8b-tetrahydro-indeno[2,1-d]oxazol-2-one 
• 184583-16-2 (3aS,8bR)-4,4-Dimethyl-3-(3-phenyl-propionyl)-3,3a,4,8b-tetrahydro-indeno[2,1-d]oxazol-2-one 

Relevant academic research and scientific papers

Cis-2-amino-3,3-dimethyl-1-indanol: Synthesis, resolution, and application as a highly efficient chiral auxiliary

The chiral amino alcohol, cis-2-amino-3,3-dimethyl-1-indanol was synthesized and resolved. Its oxazolidinone derivative was found to be a highly efficient chiral auxiliary in an asymmetric alkylation reaction.

cis-2-amino-3,3-dimethyl-1-indanol: Application as a highly efficient chiral auxiliary for the Diels-Alder reaction

The chiral oxazolidinone, derived from cis-2-amino-3,3-dimethyl-1-indanol, was found to be an efficient chiral auxiliary in the asymmetric Diels-Alder reaction.

Design, synthesis, resolution, and application of a highly efficient chiral auxiliary: cis-2-amino-3,3-dimethyl-1-indanol

The chiral amino alcohol, cis-2-amino-3,3-dimethyl-1-indanol was synthesized and resolved. Its oxazolidinone derivative was found to be a highly efficient chiral auxiliary in diastereoselective alkylation, acylation, bromination, and hydroxylation reactions.