@article {46163,
	title = {Scalable synthesis of cladosporin},
	journal = {Tetrahedron Letters},
	volume = {60},
	year = {2019},
	month = {MAR },
	pages = {831-833},
	type = {Article},
	abstract = {<p>Cladosporin, a secondary metabolite isolated from fungal sources like Cladosporium cladosporioides and Aspergillus flavus was found to exhibit selective nano-molar activity against malarial parasite Plasmodium falciparum by inhibiting parasitic protein biosynthesis. In addition, this natural product has a broad range of bioactivities including, antiparasitic, antifungal, antibacterial as well as plant growth inhibition. However, it has limited availability from the natural sources for further development. Herein, we report a modified and improved synthetic route which led us to produce this potent natural product in a gram scale. Conversion of the undesired diastereomer to desired one via Mitsunobu inversion of secondary alcohol and carbon monoxide insertion reaction towards the construction of isocoumarin unit are the key features of the present synthesis. (C) 2019 Elsevier Ltd. All rights reserved.</p>
},
	keywords = {Anti-malarials, Cladosporin, Mitsunobu, Total synthesis},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2019.02.012},
	author = {Das, Pronay and Mankad, Yash and Reddy, D. Srinivasa}
}
