Amberlyst-15 Catalyzed Cbz Protection of Amines Under Solvent-Free Conditions

Pranjal P. Bora; Khiangte Vanlaldinpuia; Samuel Lalthazuala Rokhum; Ghanashyam Bez

doi:10.1080/00397911.2010.515341

ScienceGate Book Chapters

JOURNAL ARTICLE

Amberlyst-15 Catalyzed Cbz Protection of Amines Under Solvent-Free Conditions

Pranjal P. Bora Khiangte Vanlaldinpuia Samuel Lalthazuala Rokhum Ghanashyam Bez

Year: 2011 Journal: Synthetic Communications Vol: 41 (18)Pages: 2674-2683 Publisher: Taylor & Francis

DOI: 10.1080/00397911.2010.515341

Get Full-Text PDF Get Analytical Report

Abstract

Abstract Amberlyst-15 can effectively catalyze Cbz protection of aliphatic and aromatic amines within 10–15 min under solvent-free conditions. The catalyst can be used repeatedly without loss of activity, and the reaction requires no workup and gives excellent yields.

Keywords:

Chemistry Catalysis Organic chemistry Solvent

Metrics

Cited By

0.16

FWCI (Field Weighted Citation Impact)

Refs

0.52

Citation Normalized Percentile

Is in top 1%

Is in top 10%

Citation History

Topics

Chemical Synthesis and Reactions

Physical Sciences → Chemistry → Organic Chemistry

Chemical Synthesis and Analysis

Life Sciences → Biochemistry, Genetics and Molecular Biology → Molecular Biology

Asymmetric Hydrogenation and Catalysis

Physical Sciences → Chemistry → Inorganic Chemistry

Amberlyst-15 Catalyzed Cbz Protection of Amines Under Solvent-Free Conditions

Abstract

Metrics

Citation History

Topics

Related Documents

ChemInform Abstract: Amberlyst‐15 Catalyzed Cbz Protection of Amines under Solvent‐Free Conditions.

Amberlyst-15 catalyzed acetylation of phenols and alcohols under solvent free conditions

Efficient synthesis of 5,10,15‐triarylcorroles using amberlyst 15 under solvent‐free conditions

Indium-Catalyzed N-Formylation of Amines under Solvent-Free Conditions

ChemInform Abstract: Efficient Synthesis of 5,10,15‐Triarylcorroles Using Amberlyst 15 under Solvent‐Free Conditions.