Chemical Research Letters, May 2021. The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. Name: Benzo[d][1,3]dioxole,274-09-9, Name is Benzo[d][1,3]dioxole, SMILES is C12=CC=CC=C1OCO2, belongs to pyrrolines compound. In a document, author is Schley, Daniela, introduce the new discover.
Diastereoselective cyclisation of N-alkenylideneamines into 3,4-dihydro–2H-pyrrol-1-ium halides
A number of new chiral 2-(alpha-bromoalkyl)pyrrolinium salts and 2-(alpha-selenoalkyl)pyrrolidines were synthesized by the halocyclisation and selenocyclisation, respectively, of N-(alkenylidene)alkylamines and subsequent reduction. These cyclisations were implemented in a diastereomeric fashion for the first time. Substrate control (starting imines possessing chirality in the N-alkyl or the N-alkenyl substituent) and reagent control (chiral organoselenenyl bromides) were applied. Asymmetric induction by stereocentres of the alkenylidene or double asymmetric induction by chiral selenenyl bromides on unsaturated imines with a chiral N-alkyl group resulted in diatereoselectivities up to 84:16. ((c) Wiley-VCH Verlag GmbH & Co.
Therefore, this conceptually novel strategy might open impressive avenues to establish green and sustainable chemistry platforms. 274-09-9, you can contact me at any time and look forward to more communication. Name: Benzo[d][1,3]dioxole.
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem