LITHIUM ALUMINUM AMIDES - NEW REAGENTS FOR THE SYNTHESIS OF IMINES

被引：9

作者：

SOLLADIECAVALLO, A

BENCHEQROUN, M

BONNE, F

机构：

[1] Laboratoire de Stéréochimie Organométallique associé au CNRS, EH1CS, 67008 Strasbourg

来源：

SYNTHETIC COMMUNICATIONS | 1993年 / 23卷 / 12期

关键词：

D O I：

10.1080/00397919308011266

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Aldehydes (4 eqiv.) react under mild conditions with LiAl(NHR1)4 (1 eqiv.) to give the corresponding imines in 90% yield and no polymerization was observed upon reaction of aliphatic aldehyde 3.

引用

页码：1683 / 1687

页数：5

共 7 条

[1] The preparation of unsymmetrical secondary aliphatic ammes [J].

Campbell, KN ;

Sommers, AH ;

Campbell, BK .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1944, 66 :82-84

[2]

Henry L, 1904, RECL TRAV CH PAYS-BA, V23, P401

[3] CHEMISTRY OF IMINES [J].

LAYER, RW .

CHEMICAL REVIEWS, 1963, 63 (05) :489-+

[4] INEXPENSIVE REAGENTS FOR THE SYNTHESIS OF AMIDES FROM ESTERS AND FOR REGIOSELECTIVE OPENING OF EPOXIDES [J].

SOLLADIECAVALLO, A ;

BENCHEQROUN, M .

JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (22) :5831-5834

[5] DIASTEREOSELECTIVE REDUCTION OF AN ALPHA-KETO-ESTER DERIVED FROM (-)-8-PHENYLMENTHOL - A 4-STEP SYNTHESIS OF R-HALOSTACHINE ANALOG [J].

SOLLADIECAVALLO, A ;

BENCHEQROUN, M .

TETRAHEDRON-ASYMMETRY, 1991, 2 (11) :1165-1171

[6]

STOERMER R, 1896, BER, V29, P2110

[7]

TIOLLAIS R, 1947, B SOC CHIM FR, P708

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