10-Sep-2021 News Properties and Exciting Facts About 214894-89-0

The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ‘hit’ molecules.Read on for other articles about 214894-89-0 name: 5-(Bromomethyl)-2,3-dihydro-1,4-benzodioxine

Chemical research careers are more diverse than they might first appear, as there are many different reasons to conduct research and many possible environments. name: 5-(Bromomethyl)-2,3-dihydro-1,4-benzodioxine, In a article, mentioned the application of 214894-89-0, Name is 5-(Bromomethyl)-2,3-dihydro-1,4-benzodioxine, molecular formula is C9H9BrO2

Successive nucleophilic and electrophilic allylation mediated by the bis-Boc-carbonate derived from 2-methylene-1,3-propane diol enables formation of enantiomerically enriched 2,4-disubstituted pyrrolidines. An initial enantioselective iridium-catalyzed transfer hydrogenative carbonyl C-allylation is followed by Tsuji-Trost N-allylation using 2-nitrobenzenesulfonamide. Subsequent Mitsunobu cyclization provides the N-protected 2,4-disubstituted pyrrolidines.

The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ‘hit’ molecules.Read on for other articles about 214894-89-0 name: 5-(Bromomethyl)-2,3-dihydro-1,4-benzodioxine

Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem