A short stereoselective synthesis of prepiscibactin using a SmI2-mediated Reformatsky reaction and Zn2+-induced asymmetric thiazolidine formation.
Segade, Yuri
A short stereoselective synthesis of prepiscibactin using a SmI2-mediated Reformatsky reaction and Zn2+-induced asymmetric thiazolidine formation. [electronic resource] - Organic letters Nov 2014 - 5820-3 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1523-7052
10.1021/ol502958u doi
Animals
Cysteine--chemistry
Fish Diseases--microbiology
Fishes
Iodides--chemistry
Molecular Structure
Nitriles--chemistry
Pasteurella Infections--microbiology
Pfiesteria piscicida--chemistry
Photobacterium--chemistry
Samarium--chemistry
Stereoisomerism
Thiazoles--chemical synthesis
Thiazolidines--chemistry
Zinc--chemistry
A short stereoselective synthesis of prepiscibactin using a SmI2-mediated Reformatsky reaction and Zn2+-induced asymmetric thiazolidine formation. [electronic resource] - Organic letters Nov 2014 - 5820-3 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1523-7052
10.1021/ol502958u doi
Animals
Cysteine--chemistry
Fish Diseases--microbiology
Fishes
Iodides--chemistry
Molecular Structure
Nitriles--chemistry
Pasteurella Infections--microbiology
Pfiesteria piscicida--chemistry
Photobacterium--chemistry
Samarium--chemistry
Stereoisomerism
Thiazoles--chemical synthesis
Thiazolidines--chemistry
Zinc--chemistry