Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/152879
Title: ORIENTATIONAL SELECTIVITY IN THE DIELS-ALDER REACTION OF SUBSTITUTED VINYL ACETATE WITH ALKYL SUBSTITUTED 1,3-BUTADIENE
Authors: HUM KE SIONG
Issue Date: 1973
Citation: HUM KE SIONG (1973). ORIENTATIONAL SELECTIVITY IN THE DIELS-ALDER REACTION OF SUBSTITUTED VINYL ACETATE WITH ALKYL SUBSTITUTED 1,3-BUTADIENE. ScholarBank@NUS Repository.
Abstract: Diels-Alder reaction of piperylene with methyl [ALPHA]-acetoxyacrylate was investigated. The reaction afforded high yield (~8O% ) of adduct, predominantly ( > 93% ) of one orientation, namely the ortho isomer, This is inagreement with the prediction based upon electronic theories.
URI: https://scholarbank.nus.edu.sg/handle/10635/152879
Appears in Collections:Bachelor's Theses

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
b19215307.pdf306.43 kBAdobe PDF

RESTRICTED

NoneLog In

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.