HIGHLY ENANTIOSELECTIVE BETA-LACTAM SYNTHESES VIA CHIRAL DIRHODIUM(II) CARBOXAMIDE CATALYZED CARBON-HYDROGEN INSERTION REACTIONS OF DIAZOACETAMIDES

被引：0

作者：

DOYLE, MP ^{[1
]}

KALININ, AV ^{[1
]}

机构：

[1] TRINITY UNIV,DEPT CHEM,SAN ANTONIO,TX 78212

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 1995年 / 209卷

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：104 / ORGN

共 39 条

[21] Synthesis of pyrrolizidine bases by highly diastereoselective and regioselective catalytic carbon-hydrogen insertion reactions of chiral pyrrolidinediazoacetamides
Doyle, MP
Kalinin, AV
TETRAHEDRON LETTERS, 1996, 37 (09) : 1371 - 1374
[22] ELECTRONIC AND STERIC CONTROL IN CARBON HYDROGEN INSERTION REACTIONS OF DIAZOACETOACETATES CATALYZED BY DIRHODIUM(II) CARBOXYLATES AND CARBOXAMIDES
DOYLE, MP
WESTRUM, LJ
WOLTHUIS, WNE
SEE, MM
BOONE, WP
BAGHERI, V
PEARSON, MM
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (03) : 958 - 964
[23] Asymmetric synthesis of lactones with high enantioselectivity by intramolecular carbon-hydrogen insertion reactions of alkyl diazoacetates catalyzed by chiral rhodium(II) carboxamides
1600, (113):
[24] Highly enantioselective intramolecular cyclopropanation reactions of N-allylic-N-methyldiazoacetamides catalyzed by chiral dirhodium(II) carboxamidates
Doyle, MP
Kalinin, AV
JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (06): : 2179 - 2184
[25] Highly enantioselective intramolecular cyclopropanation reactions of N-Allylic-N-methyldiazoacetamides catalyzed by chiral dirhodium(II) carboxamidates
Department of Chemistry, Trinity University, San Antonio, TX 78212, United States
J. Org. Chem., 6 (2179-2184):
[26] Quinoline β-lactams by Rh(II)-catalyzed highly steroselective intramolecular carbene insertion into a carbon-hydrogen bond
Muroni, D
Saba, A
ARKIVOC, 2005, : 1 - 7
[27] APPROACHES TO THE SYNTHESIS OF AZA ANALOGS OF THE BETA-LACTAM ANTIBIOTICS - SOME ANOMALOUS RHODIUM(II)-CATALYZED CARBENE INSERTION REACTIONS
TAYLOR, EC
DAVIES, HML
JOURNAL OF ORGANIC CHEMISTRY, 1984, 49 (01): : 113 - 116
[28] ASYMMETRIC-SYNTHESIS OF LACTONES WITH HIGH ENANTIOSELECTIVITY BY INTRAMOLECULAR CARBON-HYDROGEN INSERTION REACTIONS OF ALKYL DIAZOACETATES CATALYZED BY CHIRAL RHODIUM(II) CARBOXAMIDES
DOYLE, MP
VANOEVEREN, A
WESTRUM, LJ
PROTOPOPOVA, MN
CLAYTON, TW
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1991, 202 : 42 - ORGN
[29] A short stereoselective synthesis of (+)- and (-)-2-oxabicyclo[3.3.0]oct-6-en-3-one by intramolecular carbon-hydrogen insertion catalyzed by chiral dirhodium(II) carboxamidates
Doyle, MP
Catino, AJ
TETRAHEDRON-ASYMMETRY, 2003, 14 (07) : 925 - 928
[30] Diastereo- and enantioselective intramolecular 1,6-C-H insertion reactions of α-diazo esters catalyzed by chiral dirhodium(II) carboxylates
Ito, Motoki
Kondo, Yuji
Nambu, Hisanori
Anada, Masahiro
Takeda, Koji
Hashimoto, Shunichi
TETRAHEDRON LETTERS, 2015, 56 (11) : 1397 - 1400

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