1043476-02-3Relevant academic research and scientific papers
Scalable synthesis of enantiomerically pure cis-1,2-cyclohexanediamine derivatives and conformationally rigid 7-azabicyclo[2.2.1]heptan-2-amines
Pandey, Ganesh,Dey, Debasis,Fernandes, Rushil
, p. 4319 - 4324 (2013)
A scalable approach to the syntheses of enantiomerically pure cis-1,2-cyclohexanediamines as well as exo-and endo-7-azabicyclo[2.2.1]heptan-2- amines is reported that utilizes meso-tert-butyl 2,3-bis(phenylsulfonyl)-7- azabicyclo[2.2.1]hept-2-ene-7-carbox
Use of enantiomerically pure 7-azabicyclo[2.2.1]heptan-2-ol as a chiral template for the synthesis of aminocyclitols
Pandey, Ganesh,Tiwari, Keshri Nath,Puranik
supporting information; scheme or table, p. 3611 - 3614 (2009/05/07)
(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.
