作者:Eduardo Rodrigo、Inés Alonso、José Luis García Ruano、M. Belén Cid
DOI:10.1021/acs.joc.6b01956
日期:2016.11.18
fields such as organic synthesis and bioconjugate formation. This was demonstrated by performing a systematic assessment of its reactivity in Michael, radical, and cycloaddition reactions. Heteroaryl vinyl sulfone 3 presented excellent output in terms of reactivity and selectivity, proving superior to phenyl vinyl sulfone 1 and with clear advantages over bis-sulfone 2. This behavior might be due to the
易于获得的乙烯基砜3在有机合成和生物共轭物形成等多个领域中显示出巨大的新应用潜力。通过对其在迈克尔,自由基和环加成反应中的反应性进行系统评估,证明了这一点。杂芳基乙烯基砜3在反应性和选择性方面表现出优异的产量,被证明优于苯基乙烯基砜1,并且比双砜2具有明显的优势。此行为可能是由于四唑单元根据DFT计算施加的构象和轨道控制所致。此外,还描述了在所得产物上对Julia-Kocienski烯烃的一些替代转化。