Abstract
Bulky water-soluble 1,4-disubstituted naphthalenes react with singlet oxygen giving the usual 1,4- and the unexpected 5,8-endoperoxides and showing that the regioselectivity of the [4 + 2] cycloaddition of singlet oxygen depends on the steric hindrance of the substrate.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
