𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The Wittig reaction in the generation of organometallic compounds containing alkenes as side groups

✍ Scribed by Edward J. Miller; Carolyn A. Weigelt; Judith A. Serth; Rusydi Rusyid; Jeffery Brenner; Linda A. Luck; Michael Godlewski


Book ID
107812298
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
689 KB
Volume
440
Category
Article
ISSN
0022-328X

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Hindered organoboron groups in organic s
✍ Andrew Pelter; Keith Smith; Said Elgendy; Martin Rowlands πŸ“‚ Article πŸ“… 1989 πŸ› Elsevier Science 🌐 French βš– 210 KB

In the presence of HX, carbanions MeseBCHLiRl react with afiphatic aldehydes to give alkenes. The stereochemistry of the product alkene depends upon the nature of HX. In our previous paper1 we showed that in the presence of TFAA or NCS, anions (1) (W&H) yield ketones rather than alkenes when react

A novel carbon leaving group in the reac
✍ Cosimo Cardellicchio; Giuseppe Fracchiolla; Francesco Naso; Paolo Tortorella; Wi πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 French βš– 201 KB

The reaction of diphenyl(methoxymethyl)phosphine oxide 1 with organometallic reagents was found to lead to substitution of the methoxymethyl group. The P-phenyl substituent showed a lower propensity to undergo a displacement.

Studies in IVth group organometallic che
✍ J. G. Noltes; G. J. M. van der Kerk πŸ“‚ Article πŸ“… 2010 πŸ› Elsevier Science 🌐 English βš– 539 KB

## Abstract A number of oligomeric __p__‐phenylenesilanes containing 2‐6 silicon atoms per molecule and a series of low molecular weight poly‐__p__‐phenylenesilanes (n = 10‐30) have been prepared by Wurtz‐type condensation reactions involving appropriate combinations of __p__‐chlorophenyl‐ and chlo