Site-selective C-H alkylation of myo-inositol via organic photoredox catalysis.
Chem Commun (Camb)
; 58(71): 9934-9937, 2022 Sep 01.
Article
in En
| MEDLINE
| ID: mdl-35983711
ABSTRACT
Site-selective photoredox reactions with aromatic olefins enable direct alkylation of unprotected myo-inositol at C4. The efficacy of these reactions can be finely tuned by modifying the structures of HAT reagents. These reactions open the possibility of selective C-H alkylations of myo-inositol without the need for multi-step protection-deprotection strategies.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Alkenes
/
Inositol
Language:
En
Journal:
Chem Commun (Camb)
Journal subject:
QUIMICA
Year:
2022
Document type:
Article