Titlebook: Organomercury Compounds in Organic Synthesis; Richard C. Larock Book 1985 Springer-Verlag Berlin Heidelberg 1985 carbon.organic chemistry.

Daily-Value

Surgeon

Harass

抗原

Acylation,l route to ketones, as well as enol esters. The addition of a palladium(0) catalyst or aluminum halides often affords ketones in high yield under mild conditions. These routes to carbonyl compounds will be surveyed in this chapter on the acylation of organomercurials.

造反,叛乱

Divalent Carbon Transfer Reactions, reported reaction of this type in 1962 by Seyferth and co-workers [1], a large number of these compounds have been prepared and their application in organic synthesis explored. Their unique properties have made them particularly valuable as reagents in cyclopropane formation, ring expansion reactio

Eviction

Hydrogen and Halogen Substitution,d covering this topic. The primary emphasis of most of this work has been on studying the mechanism of electrophilic aliphatic substitution. Considerable kinetic and stereochemical information on these reactions is now available. The emphasis here, however, will be on possible synthetic applications of these reactions.

大喘气

废墟

Carbonylation,nder mild conditions. These reactions can be used to prepare a host of carbonyl-containing products, including carboxylic acids and esters, carbonates, urethanes, ureas and ketones. These reactions are the subject of this chapter.

斗志

经典