Abstract
Chemical synthesis based on Group-Assisted Purification chemistry (GAP) has been prolifically used as a powerful, greener and ecofriendly tool so far. Herein, we report hypervalent iodine (III) mediated regio- and diastereoselective aminobromination of electron-deficient olefins using group-assisted purification (GAP) method. By simply mixing the GAP auxiliary-anchored substrates with TsNH2–NBS as nitrogen/bromine sources and PhI(OAc)2 as a catalyst, a series of vicinal bromoamines with multifunctionalities were obtained in moderate to excellent yields (53–94%). The vicinal bromoamines were obtained without column chromatography and/or recrystallization simply by washing the crude mixtures with cosolvents and thus avoiding wastage of silica, solvents, time, and labor. The GAP auxiliary is recyclable and reusable.
| Original language | English |
|---|---|
| Article number | 742399 |
| Journal | Frontiers in Chemistry |
| Volume | 9 |
| DOIs | |
| State | Published - 8 Sep 2021 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© Copyright © 2021 Rahman, Zarshad, Khan, Faiz, Li and Ali.
Keywords
- aziridinium
- diastereoselectivity
- iodobenzene diacetate
- nitrogen/halogen source
- protecting groups
ASJC Scopus subject areas
- General Chemistry