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1.1.1- Trifluorides amines methyl groups

Aberle and collaborators started from a Boc-protected benzylic tyrosine derivative. The amino group was methylated (in a yield of 96%) and the corresponding amide formed (86%) after treatment with diethylaminosulfur trifluoride and an amine. [Pg.39]

Lesma and associates began their synthesis of (-b)-monomorine I (1562) with the N-Boc -protected amine 1623, a simple derivative of (5)-pyroglu-tamic acid (Scheme 205). Reaction with allyltrimethylsilane in the presence of boron trifluoride according to a reported procedure and replacement of the Boc group by Cbz produced the 2,5-n s-disubstituted pyrrolidine (—)-1624, cross-metathesis of which with methyl vinyl ketone... [Pg.299]


See other pages where 1.1.1- Trifluorides amines methyl groups is mentioned: [Pg.18]    [Pg.329]    [Pg.316]    [Pg.289]    [Pg.196]    [Pg.627]    [Pg.30]    [Pg.228]    [Pg.47]    [Pg.304]    [Pg.439]   
See also in sourсe #XX -- [ Pg.19 , Pg.98 ]




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1.1.1- Trifluorides amines

1.1.1- Trifluorides methyl groups

Amine groups

Amines methylated

Methyl amine

Methyl group

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