✦ LIBER ✦

Addition of an α-Hydroxy Acid to the Genetic Code of Bacteria

✍ Scribed by Jiantao Guo; Jiangyun Wang; J. Christopher Anderson; Peter G. Schultz

Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 584 KB
Volume: 120
Category: Article
ISSN: 0044-8249
DOI: 10.1002/ange.200704074

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Addition of an α-Hydroxy Acid to the Gen

Addition of an α-Hydroxy Acid to the Genetic Code of Bacteria

✍ Jiantao Guo; Jiangyun Wang; J. Christopher Anderson; Peter G. Schultz 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 584 KB

ChemInform Abstract: Chemoselective Ally

ChemInform Abstract: Chemoselective Allylic Addition of Allyltrichlorosilane to α-Oxocarboxylic Acids: Synthesis of Tertiary α-Hydroxy Carboxylic Acids.

✍ Zhe Wang; Guoyou Xu; Dengjin Wang; Michael E. Pierce; Pat N. Confalone 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

ChemInform Abstract: Diastereoselective

ChemInform Abstract: Diastereoselective Conjugate Addition to (+)-Camphorsulfonic Acid Derived Nitroalkenes: Synthesis of α-Hydroxy and α-Amino Acids.

✍ A. G. M. BARRETT; D. C. BRADDOCK; P. W. N. CHRISTIAN; D. PILIPAUSKAS; A. J. P. W 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 38 KB 👁 2 views

The first diastereoselective addition of

The first diastereoselective addition of an organolithium compound to α-halocarboxylic acid esters

✍ José Barluenga; Bruno Pedregal; José M. Concellón 📂 Article 📅 1993 🏛 Elsevier Science 🌐 French ⚖ 162 KB

Stereocontrolled addition to a penaldic

Stereocontrolled addition to a penaldic acid equivalent: an asymmetric of threo-β-hydroxy-L-glutamic acid

✍ Philip Garner 📂 Article 📅 1984 🏛 Elsevier Science 🌐 French ⚖ 243 KB

On the highly stereoselective addition o

On the highly stereoselective addition of lithio-acetylides to α-hydroxy-ketones

✍ Damian Dunford; Mathilde Guyader; Simon Jones; David W. Knight; Michael B. Hurst 📂 Article 📅 2008 🏛 Elsevier Science 🌐 French ⚖ 147 KB

Addition of 2 equiv of a lithio-acetylide to an unprotected a-hydroxy ketone is extremely stereoselective in examples where the two ketone substituents are relatively large.