Benzyl methoxymethyl methylamine

Juaristi, E. Quintana, D. Balderas, M. Garcia-Perez, E. Tetrahedron Asymmetry 1996, 7, 2233. [Pg.56]

Juaristi, E. Rizo, B. Natal, V. Escalante, 3. Regia, I. Tetrahedron Asymmetry 1991, 2, 821. [Pg.56]

Juaristi, E. Balderas, M. Ramirez-Quiros, Y. Tetrahedron Asymmetry 1998,9,3881. [Pg.56]

Juaristi, E. Balderas, M. Lopez-Ruiz, H. Jimenez-Pdrez, V. M. Kaiser-Carril, M. L. Ramirez-Quiros, Y. Tetrahedron Asymmetry 1999, 10, 3493. [Pg.56]

DMPU has been recommended as solvent in various alkylation reactions Juaristi, E. Murer, P. Seebach, D. Synthesis 1993,1243, and references cited therein. [Pg.56]

N-Benzyl-N-methoxymethyl-N-(tri-methylsilyl)methylamine, 31 Bis( 1,5-cyclooctadiene)nickel(0), 35 Lithium diisopropylamide, 163 N-Methyl-N, O-bis(trimethylsilyl) -hydroxylamine, 187 Titanium(IV) chloride-N-Methylani-line, 310... [Pg.362]

Benzeneselenenyl halides, 26 N-Benzyl-N-methoxymethyl-N-(trimethylsilyl)methylamine, 31 9-Bromo-9-phenylfluorene, 48 2,3-0-Isopropylidene-2,3-dihydroxy-... [Pg.390]

Benzyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium chloride (4568-71-2), 65, 26 N-Benzylidenebenzenesulfonamide (13909-34-7), 66, 203, 204, 206, 210 Benzylidenemalononitrile Malononitrile, benzylidene- Propanedinitrile, (phenylmethylene)- (2700-22-3), 65, 32 Benzyl mercaptan a-Toluenethiol Benzenemethanethiol (100-53-8), 65, 215 N-BENZYL-N-METHOXYMETHYL-N-(TRIMETHYLSlLYL)METHYLAMINE BENZENEMETHANAMINE, N-(METHOXYMETHYL)-N-[(TRlMETHYL-SILYL)METHYL]- (93102-05-7), 67, 133 1-BENZYLOXY-4-PENTEN-2-OL 4-PENTEN-2-OL. 1 -(PHENYLMETHOXY)- (58931-16-11), 69, 80... [Pg.261]

A,-Benzyl-A -methoxymethyl-(V-(trimethylsilyl)methylamine as an azo-methine ylide equivalent. [Pg.138]

S. N-Bemyl-H-methoxymethyl-S-( trimethylailyVmethylamine. A 25-mL, round-bottomed flask equipped with a stirring bar Is charged with 6.0 g (74 mmol) of a 37% aqueous formaldehyde solution (Note 4). The solution Is cooled to 0°C and 10.0 g (51.7 mmol) of N-benzyl-N-(tr1methylsilyl)methylamine Is added dropwlse with stirring. After the solution Is stirred for 10 min at 0°C, 6 ml (0.15 mol) of methanol (Note 5) Is added In one portion. Potassium carbonate (4.0 g) is added to the mixture to absorb the aqueous phase. The mixture Is stirred for 1 hr, the non-aqueous phase Is decanted, an additional... [Pg.68]

N-BENZYL-N-METHOXYMETHYL-N-(TRIMETHYLSILYL)METHYLAMINE AS AN AZOMETHINE YLIDE EQUIVALENT ... [Pg.129]

N-Benzyl-N-methoxymethyl-N- trimethylsilyl)methylamine undergoes stereo-specific cycloaddition with dimethyl maleate and fumarate. The cycloaddition behavior of an unsymmetrically substituted o-methoxysilylamine has also been examined and found to occur with high overall regioselectivity. The stereospecificity and regioselectivity of the reaction is consistent with a concerted 1,3-dipolar cycloaddition reaction. [Pg.198]

N-Benzyl-N-methoxyraethyl-N-(trimethyl silyl)methylamine Benzenemethanamine, N-(methoxymethyl)-N-[(tr1methylsilyl)methyl]- (11) (93102-05-7)... [Pg.199]

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