Dienophile Activation via Selenosulfonation: 1-(Phenylsulfonyl)cyclopentene
Author:
Affiliation:
1. The Ohio State University; Department of Chemistry; Columbus OH 43210
Publisher
John Wiley & Sons, Inc.
Reference18 articles.
1. Selenosulfonation: boron trifluoride catalyzed or thermal addition of selenosulfonates to olefins. A novel regio- and stereocontrolled synthesis of vinyl sulfones
2. Regiocontrolled synthesis of mono-, di-, and trisubstituted cyclohexenones by cycloaddition of vinyl sulfones to 1-methoxy-3-[(trimethylsilyl)oxy]-1,3-butadienes. Conversion of alkenes into effective dienophilic reagents
3. Acetylene equivalents in cycloaddition reactions
4. Conjugate addition of moderately soft anions to a vinyl sulfone
5. Cytochalasin support studies. 5. Conjugate addition of .beta.-oxo ester dianions to vinyl sulfones: a new procedure for seven-ring annulation. Synthesis of a chiral cytochalasin C intermediate via an intramolecular Diels-Alder reaction of a chiral Z diene
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