Results
1 -
8 of
8
(Click
here to explore results)
- The enantioselective synthesis of APTO and AETD: polyhydroxylated β-amino acid constituents of the microsclerodermin cyclic peptides. Emily C. Shuter, Hung Duong, Craig A. Hutton, Malcolm D. McLeod
, Org. Biomol. Chem.
, 2007
, 5
, 3183
- Highly stereoselective reduction of prochiral ketones by a bacterial reductase coupled with cofactor regeneration. Yan Ni, Chun-Xiu Li, Li-Juan Wang, Jie Zhang, Jian-He Xu
, Org. Biomol. Chem.
, 2011
, 9
, 5463
- Deep-sea natural products. Danielle Skropeta
, Nat. Prod. Rep.
, 2008
, 25
, 1131
- Asymmetric synthesis of ß-amino acids and α-substituted β-amino acids. Guiliana Cardillo, Claudia Tomasini
, Chem. Soc. Rev.
, 1996
, 25
, 117
- 15. Preparation of L-threonine. Interconversion of the four stereoisomeric α-amino-β-hydroxybutyric acids. D. F. Elliott
, J. Chem. Soc.
, 1950
, 62
- Index of author's names
, J. Chem. Soc., Abstr.
, 1923
, 124
, ii893
- 78. A new synthesis of DL-threonine. J. Attenburrow, D. F. Elliott, G. F. Penny
, J. Chem. Soc.
, 1948
, 310
- Automatic extraction–spectrofluorimetric method for the determination of imipramine in pharmaceutical preparations. Tomás Pérez-Ruiz, Carmen Martínez-Lozano, Virginia Tomás, Ciriaco Sidrach
, Analyst
, 1995
, 120
, 1103