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Ruthenium-catalyzed linear selective allylic aminations of monosubstituted allyl acetates

โœ Scribed by Motoi Kawatsura; Fumio Ata; Takuya Hirakawa; Shuichi Hayase; Toshiyuki Itoh


Publisher
Elsevier Science
Year
2008
Tongue
French
Weight
168 KB
Volume
49
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


The ruthenium-catalyzed highly linear selective allylic amination of monosubstituted allylic acetates with secondary amines was developed. The regioselectivity was controlled by the Ru 3 (CO) 12 /2-DPPBA catalyst, and a linear-type aminated product was obtained as a single regioisomer.


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โœ Nilantha S. Sirisoma; Patrick M. Woster ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 188 KB

Synthesis of potential antiparisitic 5'-aminonucloesides such as 10 could not be accomplished using standard amination procedures. Palladium(0)-catalyzed amination of cyclic allylic acetates with benzylamine or phthalimide gave the corresponding protected amines. This method was then extended to the