✦ LIBER ✦

Nucleophilic substitution at phosphoryl phosphorus

✍ Scribed by C.R. Hall; D.J.H. Smith

Publisher: Elsevier Science
Year: 1974
Tongue: French
Weight: 209 KB
Volume: 15
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)82556-9

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Nucleophilic Substitution at Phosphorus

Nucleophilic Substitution at Phosphorus Centers (SN2@P)

✍ Marc A. van Bochove; Marcel Swart; F. Matthias Bickelhaupt 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 339 KB

Nucleophilic substitution at phosphorus

Nucleophilic substitution at phosphorus in tertiary phosphines. Effect of nucleophile and medium

✍ Evan P. Kyba; Carl W. Hudson 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 200 KB

The reaction of alkyllithium reagents with tertiary phosphines has been investigated by a number of groups.' These reactions have involved the deprotonation of an aryl ring,latb mthyl,'b\*c\*d~e or bensyllfrg groups attached to

Nucleophilic substitution at an acetylen

Nucleophilic substitution at an acetylenic carbon. Carbon versus halogen attack by phosphorus nucleophiles

✍ Atsushi Fujii; Jerome I. Dickstein; Sidney I. Miller 📂 Article 📅 1970 🏛 Elsevier Science 🌐 French ⚖ 160 KB

Nucleophilic substitutions at ozonides

✍ Karl Griesbaum; Willi Volpp; Tae-Seong Huh 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 110 KB

Reactions of 3-acetoxy-3,5,5-trimethyl-1,2,4-trioxolane (z) with methanol, benzyl alcohol or phenol gave the corresponding ether ozonldes z -e. Reaction of 2 with benzyl alcohol and with acetate ion gave 5d and 2, respectfiely. -The known reactions of nucleophiles with ozonides 1 occur either by att

SE(P): Electrophilic Substitution at Pho

SE(P): Electrophilic Substitution at Phosphorus

✍ Dr. S. G. Warren 📂 Article 📅 1968 🏛 John Wiley and Sons 🌐 English ⚖ 964 KB

Stereochemistry of substitution at trico

Stereochemistry of substitution at tricovalent phosphorus

✍ Otto Dahl 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 207 KB

## Reactions of one diastereomer of a )P-NMe2 compound (La) with alcohols, phenol and amines have been shown by NMR to proceed with initial inversion at phosphorus, but the overall reactions are not stereoselective.