667870-41-9

Upstream product

• 95-14-7 1,2,3-Benzotriazole 
• 638-37-9 butanedial 
• 219897-70-8 (S)-l-(α-aminobenzyl)-2-naphthol (R,R)-tartrate 

Downstream Products

• 1042368-73-9 C₂₇H₂₉NO 
• 1283098-11-2 (7aR,10R,12S)-7a,8,9,10-tetrahydro-10-vinyl-12-phenyl-12H-naphtho[1,2-e]pyrrolo[2,1-b][1,3]oxazine 
• 1042368-66-0 C₂₇H₂₇NO 
• 1042368-64-8 C₂₆H₂₅NO 
• 1042368-71-7 C₂₆H₂₇NO 
• 1283098-17-8 (7aR,10R,12S)-7a,8,9,10-tetrahydro-10-(prop-1-ynyl)-12-phenyl-12H-naphtho[1,2-e]pyrrolo[2,1-b][1,3]oxazine 
• 1042368-68-2 C₃₂H₂₉NO 
• 1283098-18-9 (7aR,10R,12S)-7a,8,9,10-tetrahydro-10-phenyethynyl-12-phenyl-12H-naphtho[1,2-e]pyrrolo[2,1-b][1,3]oxazine 
• 1283098-16-7 (7aR,10R,12S)-7a,8,9,10-tetrahydro-10-ethynyl-12-phenyl-12H-naphtho[1,2-e]pyrrolo[2,1-b][1,3]oxazine 
• 521960-29-2 (S)-1-(phenyl(pyrrolidin-1-yl)methyl)naphthalen-2-ol 
• 500352-88-5 (7aR,12S)-12-phenyl-7a,8,9,10-tetrahydro-12H-naphtho[1,2-e]pyrrolo[2,1-b][1,3]oxazine 

Relevant academic research and scientific papers

Diastereopure Preparation of α-Benzotriazolyl 1-Azacycloalka[2,1-b] [1,3]-oxazines and their Application as Versatile Chiral Precursors

A group of diastereopure α-benzotriazolyl 1-azacycloalka[2,1-b][1,3] oxazines were prepared from non-racemic Betti base and they were employed as the versatile precursors for the preparation of chiral ligands and chiral substituted azacyclics with signifi

An improved synthesis of chiral 1-[α-(1-azacycloalkyl)benzyl]-2- naphthols

An improved synthesis of homochiral 1-[α-(1-azacycloalkyl)benzyl]-2- naphthols and 1-[α-(2-arylpiperidyl)benzyl]-2-naphthols has been achieved by employing diastereomerically pure α-benzotriazolyl 1-azacycloalka[2,1- b][1,3]oxazines as homochiral precurso