𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Some Alternative Synthetic Routes to γ- and δ-Oxo Acid Derivatives

✍ Scribed by Ferenc Csende


Publisher
John Wiley and Sons
Year
2003
Weight
50 KB
Volume
34
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthetic routes to cristatic acid and d
✍ Jack Chiarello; Madeleine M. Joullié 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 856 KB

Synthetic patha to crfrbtic add derfvutfvea are expJored and a convergent mute to the total syntbesim of tbsm moleculea in dsmcribed. Criatatic acid (l), a farneayl phenol modified by incorporation of a furan ring in ita dde chain, waa inolated fmm the fruiting bodies of AJbatreJJu~ crJAatue by Step

1,4-Reductive Addition of Hydrazoic Acid
✍ Sofia D. Koulocheri; Serkos A. Haroutounian; Costas D. Apostolopoulos; Raj K. Ch 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 261 KB 👁 1 views

γ-Oxo-α,β-unsaturated δ-lactones and lactams, which are in high yields, of the corresponding α-amino-γ-oxo-α,βunsaturated δ-lactones and -lactams, compounds of great easily accessible from their corresponding 2-furylcarbinols, were used as substrates for the 1,4-reductive addition of biological and

Electrophile-induced cyclization of γ,δ-
✍ Norbert de Kimpe; Mark Boelens; Johan Piqueur; Jan Baele 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 272 KB

Cyciiition of r,b-alkenylimines with bromine in dichloromethane gave instantaneous formation of cyclic iminium bromides, which were converted into either pyrrolidines or piperidines, depending upon the substitution pattern. This reaction has been applied in the synthesis of 2.azaspiro compounds.

ChemInform Abstract: New Synthetic Route
✍ M. J. CROSSLEY; Y. M. FUNG; E. KYRIAKOPOULOS; J. J. POTTER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 1 views

New Synthetic Routes to α-Amino Acids and γ-Oxygenated α-Amino Acids. Reductive Denitration and Oxidative Transformations of γ-Nitro-α-amino Acids. -In continuation of a recent work to synthesize γ-nitro α-amino acid derivatives, a novel approach to the title compounds such as (II), (III), (IV), (V