Diastereoselective and regioselective single-oxygen ene reaction of oxazolidine-substituted alkenes: Control through hydrogen bonding mediated by the urea functionality of chiral auxiliaries

MLA

Adam, Waldemar, et al. “Diastereoselective and Regioselective Single-Oxygen Ene Reaction of Oxazolidine-Substituted Alkenes: Control through Hydrogen Bonding Mediated by the Urea Functionality of Chiral Auxiliaries.” Journal of the American Chemical Society, vol. 122, no. 31, Aug. 2000, p. 7610. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsggo&AN=edsgcl.66457826&authtype=sso&custid=ns315887.

APA

Adam, W., Peters, K., Peters, E.-M., & Schambony, S. B. (2000). Diastereoselective and regioselective single-oxygen ene reaction of oxazolidine-substituted alkenes: Control through hydrogen bonding mediated by the urea functionality of chiral auxiliaries. Journal of the American Chemical Society, 122(31), 7610.

Chicago

Adam, Waldemar, Karl Peters, Eva-Maria Peters, and Simon B. Schambony. 2000. “Diastereoselective and Regioselective Single-Oxygen Ene Reaction of Oxazolidine-Substituted Alkenes: Control through Hydrogen Bonding Mediated by the Urea Functionality of Chiral Auxiliaries.” Journal of the American Chemical Society 122 (31): 7610. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsggo&AN=edsgcl.66457826&authtype=sso&custid=ns315887.