Cite
A new diastereoselective aza-allyl conjugate addition–Michael addition–ring closure reaction sequence and its application in the construction of six contiguous stereogenic centres.
MLA
Magdaline Koutsaplisnée Minopoulos., et al. “A New Diastereoselective Aza-Allyl Conjugate Addition–Michael Addition–ring Closure Reaction Sequence and Its Application in the Construction of Six Contiguous Stereogenic Centres.” Chemical Communications, vol. 2007, no. 34, Aug. 2007, pp. 3580–82. EBSCOhost, https://doi.org/10.1039/b707707f.
APA
Magdaline Koutsaplisnée Minopoulos., Philip C. Andrews, Steven D. Bull, Peter J. Duggan, Benjamin H. Fraser, & Paul Jensen. (2007). A new diastereoselective aza-allyl conjugate addition–Michael addition–ring closure reaction sequence and its application in the construction of six contiguous stereogenic centres. Chemical Communications, 2007(34), 3580–3582. https://doi.org/10.1039/b707707f
Chicago
Magdaline Koutsaplisnée Minopoulos., Philip C. Andrews, Steven D. Bull, Peter J. Duggan, Benjamin H. Fraser, and Paul Jensen. 2007. “A New Diastereoselective Aza-Allyl Conjugate Addition–Michael Addition–ring Closure Reaction Sequence and Its Application in the Construction of Six Contiguous Stereogenic Centres.” Chemical Communications 2007 (34): 3580–82. doi:10.1039/b707707f.