⌘+K

Pulse Explore Communities Researchers Journals

Home Communities Explore

January 1, 2012Chemical Communications

Iridium catalysed chemoselective alkylation of 2′-aminoacetophenone with primary benzyl type alcohols under microwave conditions

Shailen Bhat Visuvanathar Sridharan

View at Publisher

Ask AI

Bookmark

Share

Abstract

2'-Aminoacetophenone was chemoselectively alkylated with a range of substituted benzyl, heteroaryl alcohols to afford either the corresponding C- or N- alkylated products in good yield.

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Bhat et al. (2012) studied this question.

synapsesocial.com/papers/6a99877ed4ecc439fa157b4e https://doi.org/10.1039/c2cc31055d

View at Publisher

Ask AI

Bookmark

Share

Keep reading

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

1Borrowing Hydrogen in the Activation of AlcoholsOriginal Research · 2007 · 1,136 citations
2Transition metal catalysed reactions of alcohols using borrowing hydrogen methodologyOriginal Research · 2008 · 677 citations
3Alcohols as Electrophiles in CC Bond‐Forming Reactions: The Hydrogen Autotransfer ProcessReview · 2007 · 562 citations
4The Catalytic Amination of AlcoholsReview · 2011 · 749 citations
5Oxidative Cyclization of Amino Alcohols Catalyzed by a Cp*Ir Complex. Synthesis of Indoles, 1,2,3,4-Tetrahydroquinolines, and 2,3,4,5-Tetrahydro-1-benzazepineOriginal Research · 2002 · 252 citations

More related papers

Cp*Ir Complex-Catalyzed <i>N</i>-Heterocyclization of Primary Amines with Diols: A New Catalytic System for Environmentally Benign Synthesis of Cyclic Amines2004
Conversion of alcohols into N-alkyl anilines via an indirect aza-Wittig reaction2004
[Cp*IrCl2]2-Catalyzed Indirect Functionalization of Alcohols: Novel Strategies for the Synthesis of Substituted Indoles2007

More from Chemical Communications

Light-activated thiomaleimide crosslinking stabilizes collagen mimetic peptide triple helixThu,
Macrocyclic stibine-bridged [1.1.1] and [1.1.1.1] ferrocenophanesThu,