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Efficient synthesis of 3-alkyl indoles through regioselective ring opening of epoxides catalyzed by sulfated zirconia ☆

Paper ID Volume ID Publish Year Pages File Format Full-Text
52227 46867 2008 4 PDF Available
Title
Efficient synthesis of 3-alkyl indoles through regioselective ring opening of epoxides catalyzed by sulfated zirconia ☆
Abstract

Sulfated zirconia has been found to be an efficient catalyst for ring-opening of epoxides with nitrogen heterocycles such as indoles, pyrroles and imidazoles to afford the corresponding Friedel–Crafts alkylated derivatives in high yields and with high regioselectivity.

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Efficient synthesis of 3-alkyl indoles through regioselective ring opening of epoxides catalyzed by sulfated zirconia ☆
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Publisher
Database: Elsevier - ScienceDirect
Journal: Catalysis Communications - Volume 9, Issue 5, 20 March 2008, Pages 635–638
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
Online Support
Any Questions? feel free to contact us