Tetrahedron letters

Proline 4-hydroxylase: stereochemical course of the reaction

…, RA Field, CC Lawrence, KD Merritt, CJ Schofield

Index: Baldwin, Jack E.; Field, Robert A.; Lawrence, Christopher C.; Merritt, Kirsten D.; Schofield, Christopher J. Tetrahedron Letters, 1993 , vol. 34, # 46 p. 7489 - 7492

Full Text: HTML

Citation Number: 25

Abstract

Abstract The stereochemical course of the hydroxylation of (S)-proline by proline 4- hydroxylase from Streptomyces griseoviridus P8648 has been investigated using (2S, 4S)-[4- 2 H 1]-proline and (2S, 4R)-[4-2 H 1]-proline and found to occur with retention of stereochemistry at C-4 of proline.

Related Articles:

Total synthesis of echinocandins. I. Stereocontrolled syntheses of the constituent amino acids

[Kurokawa, Natsuko; Ohfune, Yasufumi Journal of the American Chemical Society, 1986 , vol. 108, # 19 p. 6041 - 6043]

Total synthesis of echinocandins. I. Stereocontrolled syntheses of the constituent amino acids

[Kurokawa, Natsuko; Ohfune, Yasufumi Journal of the American Chemical Society, 1986 , vol. 108, # 19 p. 6041 - 6043]

Total synthesis of echinocandins. I. Stereocontrolled syntheses of the constituent amino acids

[Kurokawa, Natsuko; Ohfune, Yasufumi Journal of the American Chemical Society, 1986 , vol. 108, # 19 p. 6041 - 6043]

Total synthesis of echinocandins. I. Stereocontrolled syntheses of the constituent amino acids

[Kurokawa, Natsuko; Ohfune, Yasufumi Journal of the American Chemical Society, 1986 , vol. 108, # 19 p. 6041 - 6043]

Synthetic studies on antifungal cyclic peptides, echinocandins. Stereoselective total synthesis of echinocandin D via a novel peptide coupling

[Kurokawa, Natsuko; Ohfune, Yasufumi Tetrahedron, 1993 , vol. 49, # 28 p. 6195 - 6222]

More Articles...