fulltext.study @t Gmail

Meso-tetraarylporphyrin catalyzed highly regioselective ring opening of epoxides with acetic acid

Paper ID Volume ID Publish Year Pages File Format Full-Text
51738 46852 2009 3 PDF Available
Title
Meso-tetraarylporphyrin catalyzed highly regioselective ring opening of epoxides with acetic acid
Abstract

Highly regioselective ring opening of styrene oxide with acetic acid in the presence of catalytic amounts of meso-tetra(4-CH3)phenyl- or meso-tetraphenylporphyrin at room temperature is reported. Under the same reaction conditions, cyclohexene oxide is more reactive than styrene oxide and gives the trans-isomer as the sole product.

First Page Preview
Meso-tetraarylporphyrin catalyzed highly regioselective ring opening of epoxides with acetic acid
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
Publisher
Database: Elsevier - ScienceDirect
Journal: Catalysis Communications - Volume 10, Issue 4, 10 January 2009, Pages 388–390
Authors
, , ,
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