Control of chemoselectivity in Dieckmann ring closures leading to tetramic acids.
Yong-Chul Jeong, Muhammad Anwar, Tuan Minh Nguyen, Benjamin Song Wei Tan, Christina Li Lin Chai, Mark G Moloney
Index: Org. Biomol. Chem. 9 , 6663, (2011)
Full Text: HTML
Abstract
An efficient strategy for the control of the chemoselectivity in Dieckmann ring closures leading to tetramic acids derived from serine and α-methyl serine is reported, and this provides pathways to diversely substituted systems from a common starting material.
Related Compounds
Related Articles:
2009-08-27
[J. Med. Chem. 52 , 5093-107, (2009)]
1993-09-01
[J. Steroid Biochem. Mol. Biol. 46(3) , 337-47, (1993)]
1992-10-01
[Acta Chem. Scand. 46(10) , 989-93, (1992)]
1988-11-01
[Int. J. Pept. Protein Res. 32(5) , 344-51, (1988)]
2006-01-01
[Acta Pol. Pharm. 63(5) , 426-9, (2006)]