@article {45599,
	title = {Total synthesis of marine natural products serinolamide A and columbamide D},
	journal = {ACS Omega},
	volume = {4},
	year = {2019},
	month = {JAN},
	pages = {1322{\textendash}1328},
	type = {Article},
	abstract = {<p>In this report, an expeditious synthesis of two new biologically active marine natural products serinolamide A and columbamide D is documented. This convergent approach involves the key steps such as hydrolytic kinetic resolution, cross metathesis, Grignard reaction, Johnson{\textendash}Claisen rearrangement, Mitsunobu, and so forth. Both of the target molecules were obtained from a common precursor (R)-7 with high enantioselectivity, less synthetic steps, and in good overall yields (serinolamide A 66\% and columbamide D 62\%).</p>
},
	doi = {10.1021/acsomega.8b03417},
	author = {Ghotekar, G. S. and Mujahid, M. and Muthukrishnan, M.}
}
