The Journal of Organic Chemistry

Stereoconservative reductive methyl-and dimethylamination of isomeric 3, 3-diarylpropenals. Synthetic and mechanistic studies on control of the stereochemistry

T Hoegberg, B Ulff

Index: Hoegberg, Thomas; Ulff, Bengt Journal of Organic Chemistry, 1984 , vol. 49, # 22 p. 4209 - 4214

Full Text: HTML

Citation Number: 8

Abstract

STEREOSPECIFIC REACTION: idine nitrogen oxidized, since both oxidation levels are indicated from the metabolites i~ olated.~ Reductive amination of carbonyl compounds with sodium cyanoborohydride is a widely used way of making amines.* However, with conjugated aldehydes this reaction has been rather scantily inve~ tigated.~~,~ The reaction has been accompanied by double bond reduction5" and formation of 1, 3-diamino ...

Related Articles:

Synthesis of 3-aryl-3-pyridylallylamines related to zimelidine via palladium-catalyzed amination

[Journal of Organic Chemistry, , vol. 46, # 17 p. 3479 - 3483]

Synthesis of 3-aryl-3-pyridylallylamines related to zimelidine via palladium-catalyzed amination

[Journal of Organic Chemistry, , vol. 46, # 17 p. 3479 - 3483]

Synthesis of pyridylallylamines related to zimelidine and their inhibition of neuronal monoamine uptake

[Journal of Medicinal Chemistry, , vol. 24, # 12 p. 1499 - 1507]

Stereoconservative reductive methyl-and dimethylamination of isomeric 3, 3-diarylpropenals. Synthetic and mechanistic studies on control of the stereochemistry

[Journal of Organic Chemistry, , vol. 49, # 22 p. 4209 - 4214]

Synthesis of 3-aryl-3-pyridylallylamines related to zimelidine via palladium-catalyzed amination

[Journal of Organic Chemistry, , vol. 46, # 17 p. 3479 - 3483]

More Articles...