ChemInform Abstract: Synthesis of Hydantoin Analogues of (2S,3R,4S)-4-Hydroxyisoleucine with...

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ChemInform 2008, 39, issue 48 ©WlLEY-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Hydantoin derivatives R 0210 Synthesis of Hydantoin Analogues of (2S,3R,4S)-4-Hydroxyisoleucine with Insuli- notropic Properties. — The first synthesis of optically pure hydantoin (V), an ana- logue of (2R,3R,4S)-4-hydroxyisoleucine, is described. Compound (V) is stable in acidic environment and stimulates the insulin secretion. — (SERGENT, D.; WANG, Q.; SASAKI, N. A.; OUAZZANI*, J.; Bioorg. Med. Chem. Lett. 18 (2008) 15, 4332-4335; Inst. Chim. Subst. Nat., CNRS, F-91198 Gif-sur-Yvette, Fr.; Eng.) — H. Toeppel 48- 123

Transcript of ChemInform Abstract: Synthesis of Hydantoin Analogues of (2S,3R,4S)-4-Hydroxyisoleucine with...

Page 1: ChemInform Abstract: Synthesis of Hydantoin Analogues of (2S,3R,4S)-4-Hydroxyisoleucine with Insulinotropic Properties.

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Hydantoin derivativesR 0210 Synthesis of Hydantoin Analogues of (2S,3R,4S)-4-Hydroxyisoleucine with Insuli-

notropic Properties. — The first synthesis of optically pure hydantoin (V), an ana-logue of (2R,3R,4S)-4-hydroxyisoleucine, is described. Compound (V) is stable in acidic environment and stimulates the insulin secretion. — (SERGENT, D.; WANG, Q.; SASAKI, N. A.; OUAZZANI*, J.; Bioorg. Med. Chem. Lett. 18 (2008) 15, 4332-4335; Inst. Chim. Subst. Nat., CNRS, F-91198 Gif-sur-Yvette, Fr.; Eng.) — H. Toeppel

48- 123

ChemInform 2008, 39, issue 48 ©WlLEY-VCH Verlag GmbH & Co. KGaA, Weinheim