Naval Bajwa, Ph.D.

Synthetic Methodology and Total Synthesis of Natural Products

Michael P. Jennings	grad student	2008	University of Alabama
(Studies towards the total synthesis of the biologically active natural product aigialomycin D and development of two novel methodologies.)

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Bajwa N, Jennings MP. (2012) A chemo- and diastereoselective ring closing metathesis macrocyclization approach to the total syntheses of aigialomycin C and D Strategies and Tactics in Organic Synthesis. 8: 153-169
Bajwa N, Jennings MP. (2008) An efficient 1,2-chelation-controlled reduction of protected hydroxy ketones via Red-Al. The Journal of Organic Chemistry. 73: 3638-41
Bajwa N, Jennings MP. (2008) Syntheses of epi-aigialomycin D and deoxy-aigialomycin C via a diastereoselective ring closing metathesis macrocyclization protocol Tetrahedron Letters. 49: 390-393
Bajwa N, Jennings MP. (2006) Efficient and selective reduction protocols of the 2,2-dimethyl-1,3-benzodioxan-4-one functional group to readily provide both substituted salicylaldehydes and 2-hydroxybenzyl alcohols. The Journal of Organic Chemistry. 71: 3646-9