2007
DOI: 10.1016/j.molcata.2007.05.004
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Direct reductive amination of aldehydes and selective reduction of α,β-unsaturated carbonyl compounds by NaBH4 in the presence of guanidine hydrochloride in water

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Cited by 44 publications
(22 citation statements)
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“…For these conversions, hydrogen can be produced as reducing agent in the presence of metal catalysts (4Á8), ZnÁAcOH (9), Et 3 SiHÁCF 3 CO 2 H (10), Bu 3 SnHÁ DMF (11), NaBH 4 along with catalysts such as various acids (12), boric acid/p-toulenesulfonic acid/ benzoic acid (13), boric acid (14), acetic acid (15), trifluoroacetic acid (16), silica-phosphoric acid (17), iodine (18), indium chloride (19), guanidine-hydrochloride (20), 12-tungstophosphoric acid (21), ionic liquids (22), titanium (IV) isopropoxide (23), and polyaniline salt (PANI) (24). In addition, there are some reports on development of electrochemical reductive amination reactions (25Á27).…”
Section: Introductionmentioning
confidence: 99%
“…For these conversions, hydrogen can be produced as reducing agent in the presence of metal catalysts (4Á8), ZnÁAcOH (9), Et 3 SiHÁCF 3 CO 2 H (10), Bu 3 SnHÁ DMF (11), NaBH 4 along with catalysts such as various acids (12), boric acid/p-toulenesulfonic acid/ benzoic acid (13), boric acid (14), acetic acid (15), trifluoroacetic acid (16), silica-phosphoric acid (17), iodine (18), indium chloride (19), guanidine-hydrochloride (20), 12-tungstophosphoric acid (21), ionic liquids (22), titanium (IV) isopropoxide (23), and polyaniline salt (PANI) (24). In addition, there are some reports on development of electrochemical reductive amination reactions (25Á27).…”
Section: Introductionmentioning
confidence: 99%
“…50 A convenient preparative procedure has been developed for the reductive alkylation with NaBH 4 in the presence of tungstophosphoric acid H 3 PW 12 O 40 Ð a strong heteropoly acid more efficient in acid catalysis than other inorganic and organic protonic acids. This acid does not induce corrosion and is readily separated from the reaction products.…”
Section: Methodsmentioning
confidence: 99%
“…Because, other approaches such as: the reduction of nitro, cyano, azide, carboxamide compounds or the alkylation of amines are often problemssuch as: harsh reaction conditions, overalkylation, low chemical selectivity and generally poor yields. The reductive aminationreactionhas been carried out by sodium borohydridewith different reducing system [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15] .But, in continuing our efforts for the development of new reducing systems [16][17][18][19][20][21][22][23][24][25][26][27][28] ,in this context, we have reported the reductive amination reaction of aldehydes with anilines by NaBH 4 /C system in THF.…”
Section: Introductionmentioning
confidence: 99%