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Volumn 44, Issue 14, 2012, Pages 2162-2172
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Click-BINOLs: A new class of tunable ligands for asymmetric catalysis
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Author keywords
'click' chemistry; aldehydes; alkynes; asymmetric catalysis; BINOL ligands; diethylzinc additions; Lewis acids
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Indexed keywords
ALKYNES;
ASYMMETRIC CATALYSIS;
CATALYTIC BEHAVIOR;
DIETHYLZINC ADDITION;
FINE TUNING;
LEWIS ACID;
LEWIS ACID CATALYSIS;
REACTION CONDITIONS;
SUBSTITUTION PATTERNS;
TRIAZOLE RING;
TUNABLE LIGANDS;
ACETYLENE;
ALDEHYDES;
CATALYSIS;
NITROGEN COMPOUNDS;
ORGANIC COMPOUNDS;
LIGANDS;
1 (2 CHLOROPHENYL)PROPAN 1 OL;
1 (3 CHLOROPHENYL)PROPAN 1 OL;
1 (4 CHLOROPHENYL)PROPAN 1 OL;
1 (4 FLUOROPHENYL)PROPAN 1 OL;
1 (4 METHOXYPHENYL)PROPAN 1 OL;
1 (NAPHTHALEN 1 YL)PROPAN 1 OL;
1 (NAPHTHALEN 2 YL)PROPAN 1 OL;
1 CYCLOHEXYLPROPAN 1 OL;
1 PHENYLPROPAN 1 OL;
2,2' DIHYDROXY 1,1' BINAPHTHYL;
3 (4 MESITYL 1H 1,2,3 TRIAZOL 1 YL) 2,2' DIHYDROXY 1,1' BINAPHTHYL;
3 (4 PHENYL 1H 1,2,3 TRIAZOL 1 YL) 2,2' DIHYDROXY 1,1' BINAPHTHYL;
3 [(4 PHENYL 1H 1,2,3 TRIAZOL 1 YL)METHYL] 2,2' DIHYDROXY 1,1' BINAPHTHYL;
3,3' BIS(1H 1,2,3 TRIAZOL 1 YL) 2,2' DIHYDROXY 1,1' BINAPHTHYL;
3,3' BIS(4 PHENYL 1H 1,2,3 TRIAZOL 1 YL) 2,2' DIHYDROXY 1,1' BINAPHTHYL;
3,3' BIS(5 PHENYL 1H 1,2,3 TRIAZOL 1 YL) 2,2' DIHYDROXY 1,1' BINAPHTHYL;
3,3' BIS[(4 PHENYL 1H 1,2,3 TRIAZOL 1 YL)METHYL] 2,2' DIHYDROXY 1,1' BINAPHTHYL;
3,3' BIS[4 (2,3,5,6 TETRAFLUORO 4 METHOXYPHENYL) 1H 1,2,3 TRIAZOL 1 YL] 2,2' DIHYDROXY 1,1' BINAPHTHYL;
3,3' BIS[4 (ADAMANTAN 1 YL) 1H 1,2,3 TRIAZOL 1 YL] 2,2' DIHYDROXY 1,1' BINAPHTHYL;
3,3' BIS[4 (ANTHRACEN 9 YL) 1H 1,2,3 TRIAZOL 1 YL] 2,2' DIHYDROXY 1,1' BINAPHTHYL;
3,3' BIS[4 (PYRIDIN 2 YL) 1H 1,2,3 TRIAZOL 1 YL] 2,2' DIHYDROXY 1,1' BINAPHTHYL;
3,3' BIS[4 (TERT BUTYL) 1H 1,2,3 TRIAZOL 1 YL] 2,2' DIHYDROXY 1,1' BINAPHTHYL;
3,3' BIS[4 [(DIMETHYLAMINO)NETHYL] 1H 1,2,3 TRIAZOL 1 YL] 2,2' DIHYDROXY 1,1' BINAPHTHYL;
ALDEHYDE;
ALKYNE;
DIETHYLZINC;
LEWIS ACID;
LIGAND;
TRIAZOLE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ADDITION REACTION;
ARTICLE;
ASYMMETRIC CATALYSIS;
CHEMICAL STRUCTURE;
CLICK CHEMISTRY;
CYCLOADDITION;
ENANTIOSELECTIVITY;
SUBSTITUTION REACTION;
SYNTHESIS;
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EID: 84863722015
PISSN: 00397881
EISSN: 1437210X
Source Type: Journal
DOI: 10.1055/s-0031-1291009 Document Type: Article |
Times cited : (20)
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References (19)
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