@article {43851,
	title = {Biomimetic total synthesis of angiopterlactone B and other potential natural products},
	journal = {Organic Letters},
	volume = {19},
	year = {2017},
	month = {JUL},
	pages = {3564-3567},
	type = {Article},
	abstract = {A one-pot biomimetic synthesis of (-)-angiopterlactone B and its enantiomer (+)-angiopterlactone B has been accomplished via TBAF-catalyzed tandem ring contraction followed by oxa-Michael/Michael addition sequence. Comparison of specific optical rotations, absolute configurations, and CD spectra of natural, synthesized (-)-angiopterlactone B and (+)-angiopterlactone B unequivocally proves that the isolated angiopterlactone B must be levorotatory. Synthesis of hitherto undiscovered natural products 18 and 20 and analogues of angiopterlactone B demonstrate the versatility of this method.},
	doi = {10.1021/acs.orglett.7b01525},
	author = {Kotammagari, Tharun K. and Gonnade, Rajesh G. and Bhattacharya, Asish K.}
}
