Cite
Tandem Claisen rearrangement and ruthenium catalyzed enyne bond reorganization as a route to the synthesis of tricyclic 1,8-naphthyridinones
MLA
Majumdar, K. C., et al. “Tandem Claisen Rearrangement and Ruthenium Catalyzed Enyne Bond Reorganization as a Route to the Synthesis of Tricyclic 1,8-Naphthyridinones.” Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry, vol. 47, no. 13, Mar. 2006, pp. 2111–13. EBSCOhost, https://doi.org/10.1016/j.tetlet.2006.01.132.
APA
Majumdar, K. C., Rahaman, H., Islam, R., & Roy, B. (2006). Tandem Claisen rearrangement and ruthenium catalyzed enyne bond reorganization as a route to the synthesis of tricyclic 1,8-naphthyridinones. Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry, 47(13), 2111–2113. https://doi.org/10.1016/j.tetlet.2006.01.132
Chicago
Majumdar, K.C., H. Rahaman, R. Islam, and B. Roy. 2006. “Tandem Claisen Rearrangement and Ruthenium Catalyzed Enyne Bond Reorganization as a Route to the Synthesis of Tricyclic 1,8-Naphthyridinones.” Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry 47 (13): 2111–13. doi:10.1016/j.tetlet.2006.01.132.