Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
September 15, 2010Organic Letters

Hofmann Rearrangement of Carboxamides Mediated by Hypervalent Iodine Species Generated in Situ from Iodobenzene and Oxone: Reaction Scope and Limitations

View Full Paper
Ask AI
Bookmark
Share

Authors

AZAleksandra A. ZagulyaevaIntarcia Therapeutics (United States)CBChristopher T. BanekUniversity of MinnesotaMYMekhman S. YusubovSt Petersburg University

Discussion

Loading...

Member takes

Overview

Key Points

Key points are not available for this paper at this time.

Cite This Study

Zagulyaeva et al. (2010) studied this question.

synapsesocial.com/papers/6a02fc3b67f6ea5cc8757507https://doi.org/10.1021/ol101993q
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Conversion of aliphatic amides into amines with [I,I-bis(trifluoroacetoxy)iodo]benzene. 1. Scope of the reaction1984 · 177 citations
  2. 2Rearrangement of Nα-Protected l -Asparagines with Iodosobenzene Diacetate. A Practical Route to β-Amino- l -alanine Derivatives1997 · 99 citations
  3. 3Oxidative Dearomatization of Phenols: Why, How and What For?2008 · 461 citations
  4. 4The Enantiospecific Synthesis of an Isoxazoline. A RGD Mimic Platelet GPIIb/IIIa Antagonist1997 · 61 citations
  5. 5Direct conversion of long-chain carboxamides to alkylammonium tosylates with hydroxy(tosyloxy)iodobenzene, a notable improvement over the classical Hofmann reaction1988 · 40 citations