1043475-93-9

Upstream product

• 1043475-96-2 C₃₁H₃₃NO₆S 
• 1312772-02-3 (1S,3S,4R,4'R,5'R)-tert-butyl 4',5'-diphenyl-3-(phenylsulfonyl)-7-azaspiro[bicyclo[2.2.1]hept[5]ene-2,2'-[1,3]dioxolane]-7-carboxylate 
• 1312775-57-7 (1S,3R,4R,4'R,5'R)-tert-butyl 4',5'-diphenyl-3-(phenylsulfonyl)-7-azaspiro[bicyclo[2.2.1]hept[5]ene-2,2'-[1,3]dioxolane]-7-carboxylate 

Downstream Products

• 1043476-00-1 (1S,3S,4R)-tert-butyl 2-hydroxy-3-(phenylsulfonyl)-7-azabicyclo[2.2.1]heptane-7-carboxylate 
• 1043476-02-3 (1S,2S,3R,4R)-tert-butyl 2-hydroxy-3-(phenylsulfonyl)-7-azabicyclo[2.2.1]heptane-7-carboxylate 

Relevant academic research and scientific papers

A temperature-guided diastereoselectivity switch during the desymmetrization of meso-7-azabicyclo[2.2.1]heptadiene: New strategy towards the synthesis of aminocyclitols

Strike while the iron is hot: A temperature-guided diastereoselectivity switch has been observed in the desymmetrization of meso-7-azabicyclic alkadiene. Both enantiomeric forms of this bicyclic structural framework are formed by using either of the enant

Use of enantiomerically pure 7-azabicyclo[2.2.1]heptan-2-ol as a chiral template for the synthesis of aminocyclitols

(Chemical Equation Presented) Using enantiopure 7-azabicyclo[2.2.1]heptane- 2-ol, the synthesis of cis- as well as trans-2-aminocyclohexanols, dihydroconduramine E-1, and ent-conduramine F-1 has been described.