Synthesis of N-Tosyl Allylic Amines from Substituted Alkenes via Vanadoxaziridine Catalysis

  • Rufai Madiu
  • , Erin L. Doran
  • , Jenna M. Doran
  • , Ali A. Pinarci
  • , Kiran Dhillon
  • , Dominic A. Rivera
  • , Amari M. Howard
  • , James L. Stroud
  • , Dylan A. Moskovitz
  • , Steven J. Finneran
  • , Alyssa N. Singer
  • , Morgan E. Rossi
  • , Gustavo Moura-Letts

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Herein, we report the catalytic allylic amination of α-methylalkenes with V2O3Dipic2(HMPA)2 and chloramine T as the quantitative source of N. The reaction works with high yields and stereoselectivities for α-methylalkenes. A proposed tosylnitrene-free catalytic cycle involving the formation of vanadoxaziridine complex 1 as the active catalyst and aminovanadation across the substrate as the rate-determining step has been proposed. Initial kinetic and competition experiments provide evidence for the proposed mechanism.

Original languageEnglish (US)
Pages (from-to)4001-4008
Number of pages8
JournalJournal of Organic Chemistry
Volume89
Issue number6
DOIs
StatePublished - Mar 15 2024

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Fingerprint

Dive into the research topics of 'Synthesis of N-Tosyl Allylic Amines from Substituted Alkenes via Vanadoxaziridine Catalysis'. Together they form a unique fingerprint.

Cite this