Enantioselective synthesis of the optically active alpha-methylene-beta-hydroxy esters, equivalent compounds to Morita-Baylis-Hillman adducts, using successive asymmetric aldol reaction and oxidative deselenization

MLA

Shiina, Isamu, et al. “Enantioselective Synthesis of the Optically Active Alpha-Methylene-Beta-Hydroxy Esters, Equivalent Compounds to Morita-Baylis-Hillman Adducts, Using Successive Asymmetric Aldol Reaction and Oxidative Deselenization.” Journal of Organic Chemistry, vol. 70, no. 20, Sept. 2005, p. 8103. 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.141787177&authtype=sso&custid=ns315887.

APA

Shiina, I., Yamai, Y., & Shmazaki, T. (2005). Enantioselective synthesis of the optically active alpha-methylene-beta-hydroxy esters, equivalent compounds to Morita-Baylis-Hillman adducts, using successive asymmetric aldol reaction and oxidative deselenization. Journal of Organic Chemistry, 70(20), 8103.

Chicago

Shiina, Isamu, Yu-suke Yamai, and Takahisa Shmazaki. 2005. “Enantioselective Synthesis of the Optically Active Alpha-Methylene-Beta-Hydroxy Esters, Equivalent Compounds to Morita-Baylis-Hillman Adducts, Using Successive Asymmetric Aldol Reaction and Oxidative Deselenization.” Journal of Organic Chemistry 70 (20): 8103. 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.141787177&authtype=sso&custid=ns315887.