𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of γ-Lactones and Ascorbic Acid Analogues by Diastereoselective Hydrogenation of α-Hydroxy-γ-alkylidenebutenolides

✍ Scribed by Peter Langer; Nehad N. R. Saleh; Valentin Köhler

Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
316 KB
Volume
2002
Category
Article
ISSN
1434-193X

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: From Sugar Lactones
ChemInform Abstract: From Sugar Lactones to Stereodefined γ-Alkylidenebutenolides — Synthesis of Analogues of the γ-Alkylidenebutenolide Antibiotics Lissoclinolide and Tetrenolin.
✍ F. C. GOERTH; A. UMLAND; R. BRUECKNER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 40 KB

From Sugar Lactones to Stereodefined γ-Alkylidenebutenolides -Synthesis of Analogues of the γ-Alkylidenebutenolide Antibiotics Lissoclinolide and Tetrenolin. -Analogues of the antibiotics tetrenolin (XI) and lissoclinolide (XII) are prepared in order to study the influence of the configuration of t

ChemInform Abstract: Efficient Synthesis
ChemInform Abstract: Efficient Synthesis of γ-Oxo- and γ-Hydroxy-α-amino Acids.
✍ B. MERLA; H.-J. GRUMBACH; N. RISCH 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB

Efficient Synthesis of γ-Oxo-and γ-Hydroxy-α-amino Acids. -Reduction of aminoester (Va) with Zn(BH 4 ) 2 permits intermediate isolation of the γ-hydroxy derivative, which is converted to lactone (IX) during silica gel chromatography. -(MERLA, B.;