Abstract
Abstract (−)-Norephedrine and (−)-norpseudoephedrine undergo condensation with a wide variety of 1,2-diketones to yield the corresponding 2-hydroxy-5,6-dihydro-2H-1,4-oxazines with high regio- and stereoselectivity. The X-ray structure analysis of five of the compounds studied shows that the stereochemistry at the newly formed stereogenic center is S in all cases.
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
