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Sulfur and selenium reagents for electrophilic addition

CHAPTER 4 ELECTROPHILIC ADDITIONS TO CARBON-CARBON MULTIPLE BONDS [Pg.156]

The stereospecific trans addition to norbornene is a particularly interesting reaction. Neither carbonium ion rearrangements nor the syn addition seen with many other electrophilic reagents is observed. These results, which are indicative [Pg.156]

The reaction of phenylselenenyl chloride or / -phenylselenophthalimide with unsaturated alcohols leads to cyclization and formation of /3-phenylselenenyl ethers. [Pg.157]

Reaction of alcoholic solutions of alkenes with potassium selenocyanate and [Pg.157]

This reaction proceeds by the oxidative generation of an electrophilic species, probably N=C—Se—Cl, which could be formed as a result of oxidation by Cu(II). [Pg.157]

Scheme 4.3. Sulfur and Selenium Reagents for Electrophilic Addition Reactions... Scheme 4.3. Sulfur and Selenium Reagents for Electrophilic Addition Reactions...
See other pages where Sulfur and selenium reagents for electrophilic addition is mentioned: [Pg.821]    [Pg.821]    [Pg.289]    [Pg.142]    [Pg.476]    [Pg.330]    [Pg.8]    [Pg.8]    [Pg.285]   


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And selenium addition

Electrophilic Sulfur and Selenium Reagents

Electrophilic addition and

Electrophilic selenium

Electrophilic sulfur reagent

Electrophilicity, and

For electrophilic addition

Reagent addition

Reagent electrophilic

Selenium electrophile

Selenium reagents

Sulfur Reagents

Sulfur electrophiles

Sulfur electrophilic

Sulfurization reagents

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