[GRAPHICS] Various five and six membered N-alkyl lactams were reduced to the corresponding cyclic amines using lithium N,N-dialkylaminoborohydrides (LAB), Most of the reductions were essentially complete after refluxing in THF for 2 h, The cyclic amine products were easily isolated after an aqueous workup in very good to excellent yields. It is possible to selectively reduce most functional groups, such as esters, in the presence of a lactam using LAB reagents.
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Kyoto Univ, Grad Sch Engn, Div Synthet Chem & Biol Chem, Sakyo Ku, Kyoto 60601, JapanKyoto Univ, Grad Sch Engn, Div Synthet Chem & Biol Chem, Sakyo Ku, Kyoto 60601, Japan
Kuwano, R
;
Takahashi, M
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Kyoto Univ, Grad Sch Engn, Div Synthet Chem & Biol Chem, Sakyo Ku, Kyoto 60601, JapanKyoto Univ, Grad Sch Engn, Div Synthet Chem & Biol Chem, Sakyo Ku, Kyoto 60601, Japan
Takahashi, M
;
Ito, Y
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Kyoto Univ, Grad Sch Engn, Div Synthet Chem & Biol Chem, Sakyo Ku, Kyoto 60601, JapanKyoto Univ, Grad Sch Engn, Div Synthet Chem & Biol Chem, Sakyo Ku, Kyoto 60601, Japan
机构:
Kyoto Univ, Grad Sch Engn, Div Synthet Chem & Biol Chem, Sakyo Ku, Kyoto 60601, JapanKyoto Univ, Grad Sch Engn, Div Synthet Chem & Biol Chem, Sakyo Ku, Kyoto 60601, Japan
Kuwano, R
;
Takahashi, M
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机构:
Kyoto Univ, Grad Sch Engn, Div Synthet Chem & Biol Chem, Sakyo Ku, Kyoto 60601, JapanKyoto Univ, Grad Sch Engn, Div Synthet Chem & Biol Chem, Sakyo Ku, Kyoto 60601, Japan
Takahashi, M
;
Ito, Y
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Kyoto Univ, Grad Sch Engn, Div Synthet Chem & Biol Chem, Sakyo Ku, Kyoto 60601, JapanKyoto Univ, Grad Sch Engn, Div Synthet Chem & Biol Chem, Sakyo Ku, Kyoto 60601, Japan