✦ LIBER ✦

An appreciation of Arthur Birch, 1915–1995

✍ Scribed by John M. Brown; Bernard T. Golding; D.H.R. Barton

Publisher: Elsevier Science
Year: 1997
Tongue: French
Weight: 78 KB
Volume: 53
Category: Article
ISSN: 0040-4020
DOI: 10.1016/s0040-4020(97)89737-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The steric course of proton elimination

The steric course of proton elimination in conversion of a tricarbonylcyclohexadieneiron carbinol into an endocyclic cation

✍ B.M.Ratnayake Bandara; Arthur J. Birch 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 211 KB

Organometallic compounds in organic synt

Organometallic compounds in organic synthesis. An equivalent of aromatic nucleophilic substitution by reactions of tricarbonylcyclohexadienyliumiron salts with O-silylated enolates: a novel arylation in the 2-position of carbonyl compounds.

✍ Lawrence F. Kelly; Acharan S. Narula; Arthur J. Birch 📂 Article 📅 1980 🏛 Elsevier Science 🌐 French ⚖ 255 KB

surmnary: TricarbonylcycZohexudienyZiwniron sdts are synthetGaZZy equivaZent to specifieuZZy suhtituted phenyE cationa. More extensive ability to form carbon-carbon bonds with aromatic rings would enlarge the scope of useful synthetic methods.1 Nucleophilic substitution of aryl halides by carbon nuc

The first full resolution of 2-methoxytr

The first full resolution of 2-methoxytricarbonylcyclohexadienyliron hexafluorophosphate, an example of a synthetic organic equivalent in the series of chiral cyclohex-2-enone-4-cations.

✍ B.M.Ratnayake Bandara; Arthur J. Birch; Lawrence F. Kelly; T.Chak Khor 📂 Article 📅 1983 🏛 Elsevier Science 🌐 French ⚖ 196 KB