Cite

trans-3-n-propyl-L-proline is a highly favorable, conformationally restricted replacement for methionine in the C-terminal tetrapeptide of cholecystokinin. Stereoselective synthesis of 3-allyl- and 3-n-propyl-L-proline derivatives from 4-hydroxy-L-proline

MLA

C. A. W. Wolfram, et al. “Trans-3-n-Propyl-L-Proline Is a Highly Favorable, Conformationally Restricted Replacement for Methionine in the C-Terminal Tetrapeptide of Cholecystokinin. Stereoselective Synthesis of 3-Allyl- and 3-n-Propyl-L-Proline Derivatives from 4-Hydroxy-L-Proline.” Journal of Medicinal Chemistry, vol. 34, no. 1, Jan. 1991. 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.dedup.....aaa67ce53be3da20a20a94fad6200f41&authtype=sso&custid=ns315887.



APA

C. A. W. Wolfram, David S. Garvey, Catherine S. May, David G. Witte, Chun Wel Lin, Thomas R. Miller, Mark W. Holladay, & Alex M. Nadzan. (1991). trans-3-n-propyl-L-proline is a highly favorable, conformationally restricted replacement for methionine in the C-terminal tetrapeptide of cholecystokinin. Stereoselective synthesis of 3-allyl- and 3-n-propyl-L-proline derivatives from 4-hydroxy-L-proline. Journal of Medicinal Chemistry, 34(1).



Chicago

C. A. W. Wolfram, David S. Garvey, Catherine S. May, David G. Witte, Chun Wel Lin, Thomas R. Miller, Mark W. Holladay, and Alex M. Nadzan. 1991. “Trans-3-n-Propyl-L-Proline Is a Highly Favorable, Conformationally Restricted Replacement for Methionine in the C-Terminal Tetrapeptide of Cholecystokinin. Stereoselective Synthesis of 3-Allyl- and 3-n-Propyl-L-Proline Derivatives from 4-Hydroxy-L-Proline.” Journal of Medicinal Chemistry 34 (1). 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.dedup.....aaa67ce53be3da20a20a94fad6200f41&authtype=sso&custid=ns315887.