Cite
Dihydromyrcenol carbonylation catalyzed by palladium–tin precursors: selectivity of the reaction drawn by the experimental conditions and the co-reactants
MLA
Géraldine Lenoble, et al. “Dihydromyrcenol Carbonylation Catalyzed by Palladium–tin Precursors: Selectivity of the Reaction Drawn by the Experimental Conditions and the Co-Reactants.” Journal of Organometallic Chemistry, Feb. 2002, pp. 12–18. 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=edsair&AN=edsair.doi...........65f2a42a0fed34d5ddad10bd9d9e09de&authtype=sso&custid=ns315887.
APA
Géraldine Lenoble, Philippe Kalck, & Martine Urrutigoïty. (2002). Dihydromyrcenol carbonylation catalyzed by palladium–tin precursors: selectivity of the reaction drawn by the experimental conditions and the co-reactants. Journal of Organometallic Chemistry, 12–18.
Chicago
Géraldine Lenoble, Philippe Kalck, and Martine Urrutigoïty. 2002. “Dihydromyrcenol Carbonylation Catalyzed by Palladium–tin Precursors: Selectivity of the Reaction Drawn by the Experimental Conditions and the Co-Reactants.” Journal of Organometallic Chemistry, February, 12–18. 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=edsair&AN=edsair.doi...........65f2a42a0fed34d5ddad10bd9d9e09de&authtype=sso&custid=ns315887.