Reaction of dichlorocarbene with 1-(2,4,6-tri-t-butylphenyl)-1-phosphaallenes
✍ Scribed by Masaaki Yoshifuji; Manabu Shibata; Kozo Toyota; Ikuko Miyahara; Ken Hirotsu
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 536 KB
- Volume
- 5
- Category
- Article
- ISSN
- 1042-7163
No coin nor oath required. For personal study only.
✦ Synopsis
I - (2,4,-l -phosphaallene reacted with dichlorocarbene to give 2-dichloromethylene-l-(2,4,6-tri-t-butylphenyl)-l -phosphirane. The structure was confirmed by X-ray crystal structure analysis. A similar isomerization product was obtained in the reaction of dichlorocarbene with 3-phenyl-l-(2,4,6-trit-butylpheny1)-1 -phosphaallene.
📜 SIMILAR VOLUMES
## Abstract Detailed ^1^__H__‐, ^13^__C__‐, and ^31^__P__ NMR studies of 1‐__t__‐butyl‐3‐methyl‐2,4‐bis(2,4,6‐tri‐__t__‐butylphenyl)‐1,3‐diphosphacyclobutane‐2,4‐diyl reveal several unusual coupling constants together with recognition of the diastereotopicity of the compound. These new data support
Dibenzocycloheptenylidene (2,4,6-tri-t-butylphenyl)phosphine and fluorenylidene(2,4,6-tri-t-butylphenyl)phosphine were prepared by the reactions of lithium silylphosphide with benzosuberenone and fluorenone, respectively. The reactions of the phosphines with sulfur were carried out to compare the re
## Abstract The reactions of (__E__)‐bis(2,4,6‐tri‐tert‐butylphenyl)diphosphene with tetrachloro‐o‐benzoquinone gave two products of interest, a spirophosphorane and a 1,3,2‐dioxaphospholane, indicating cleavage of the P=P bond. The structures were determined by X‐ray crystallographic analyses. © 2