- 117037-30-6
-
Baker's yeast mediated biohydrogenation of sulphur-functionalised methacrolein derivatives. Stereochemical aspects of the reaction and preparation of the two enantiomers of useful C4 bifunctional chiral synthons
-
Tetrahedron Asymmetry p. 2191 - 2196
(2007/10/03)
- File number:2
-

- 117048-15-4
-
N1-hydroxylated derivatives of chlorpropamide and its analogs as inhibitors of aldehyde dehydrogenase in vivo
-
Journal of Medicinal Chemistry p. 3641 - 3647
(2007/10/02)
- File number:2
-

- 117065-96-0
-
ENANTIOSELECTIVE CYCLIZATION OF CHIRAL BUTANE-1,4-DIOLS TO CHIRAL TETRAHYDROFURANS: SYNTHESIS OF CHIRAL TRANS-2-(3-METHOXY-5-METHYLSULFONYL-4-PROPOXYPHENYL-5-(3,4,5-TRIMETHOXYPHENYL)TETRAHYDROFURAN (L-659,989), A POTENT PAF-RECEPTOR ANTAGONIST
-
Tetrahedron Letters p. 6211 - 6214
(2007/10/02)
- File number:1
-

- 117065-98-2
-
Dynamic light scattering evidence for a ligand-induced motion between the two domains of glucoamylase G1 of Aspergillus niger with heterobivalent substrate analogues
-
Angewandte Chemie - International Edition p. 974 - 977
(2007/10/03)
- File number:2
-

- 10139-04-5
-
Facile synthesis of nitrophenyl 2-acetamido-2-deoxy-α-D- mannopyranosides from ManNAc-oxazoline
-
Beilstein Journal of Organic Chemistry p. 428 - 432
(2012/05/05)
- File number:5
-

- 1013932-65-4
-
The controllable C2 arylation and C3 diazenylation of indoles with aryltriazenes under ambient conditions
-
New Journal of Chemistry p. 9255 - 9259
(2019/06/17)
- File number:13
-

- 101399-94-4
-
9,11-Epoxy-9-homoprosta-5-enoic acid analogues as thromboxane A2 receptor antagonists
-
Journal of Medicinal Chemistry p. 1741 - 1748
(2007/10/02)
- File number:1
-

- 101399-96-6
-
9,11-Epoxy-9-homoprosta-5-enoic acid analogues as thromboxane A2 receptor antagonists
-
Journal of Medicinal Chemistry p. 1741 - 1748
(2007/10/02)
- File number:1
-

- 101400-19-5
-
Synthesis of methyl hexa-O-acetylacarviosin and the 6-acetoxy analogue
-
Carbohydrate Research p. 486 - 492
(2007/10/02)
- File number:2
-

- 1014-00-2
-
Pyran Annelation: An Effective Route to a Tricyclic Dienone
-
Journal of Organic Chemistry p. 346 - 349
(2007/10/02)
- File number:1
-

- 101400-21-9
-
Synthesis of methyl hexa-O-acetylacarviosin and the 6-acetoxy analogue
-
Carbohydrate Research p. 486 - 492
(2007/10/02)
- File number:2
-

- 101400-25-3
-
Synthesis of methyl α- and β-aminofluorodeoxypyranosides
-
Tetrahedron Letters p. 5619 - 5622
(2007/10/02)
- File number:2
-

- 101402-32-8
-
CYCLOADDITIONS OF N-BENZYLIDENEAMINOACETONITRILE AS A SYNTHETIC EQUIVALENT OF METHANENITRILE BENZZLIDE
-
Chemistry Letters p. 1601 - 1604
(2007/10/02)
- File number:4
-

- 101402-37-3
-
Regioselective Cycloadditions of N-Protonated Azomethine Ylides and 2-Azaallyl Anions Generated from N-(Silylmethyl) Thioimidates, Synthetic Equivalents of Nonstabilized Nitrile Ylides
-
Journal of Organic Chemistry p. 2523 - 2530
(2007/10/02)
- File number:4
-

- 101402-44-2
-
Regioselective Cycloadditions of N-Protonated Azomethine Ylides and 2-Azaallyl Anions Generated from N-(Silylmethyl) Thioimidates, Synthetic Equivalents of Nonstabilized Nitrile Ylides
-
Journal of Organic Chemistry p. 2523 - 2530
(2007/10/02)
- File number:4
-

- 101402-45-3
-
Regioselective Cycloadditions of N-Protonated Azomethine Ylides and 2-Azaallyl Anions Generated from N-(Silylmethyl) Thioimidates, Synthetic Equivalents of Nonstabilized Nitrile Ylides
-
Journal of Organic Chemistry p. 2523 - 2530
(2007/10/02)
- File number:3
-

- 101402-48-6
-
A New and General Route to N-Protonated Azomethine Ylides from N-(Silylmethyl)amidines and -thioamides. Cycloaddition of Synthetic Equivalents of Nitrile Ylides
-
Journal of Organic Chemistry p. 1997 - 2004
(2007/10/02)
- File number:1
-

- 101411-53-4
-
Long-acting dihydropyridine calcium antagonists. 6. Structure-activity relationships around 4-(2,3-dichlorophenyl)-3-(ethoxycarbonyl)-2-[(2-hydroxyethoxy) methyl]-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine
-
Journal of Medicinal Chemistry p. 19 - 24
(2007/10/02)
- File number:4
-

- 101411-54-5
-
Long-acting dihydropyridine calcium antagonists. 6. Structure-activity relationships around 4-(2,3-dichlorophenyl)-3-(ethoxycarbonyl)-2-[(2-hydroxyethoxy) methyl]-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine
-
Journal of Medicinal Chemistry p. 19 - 24
(2007/10/02)
- File number:1
-

- 101411-57-8
-
Long-acting dihydropyridine calcium antagonists. 6. Structure-activity relationships around 4-(2,3-dichlorophenyl)-3-(ethoxycarbonyl)-2-[(2-hydroxyethoxy) methyl]-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine
-
Journal of Medicinal Chemistry p. 19 - 24
(2007/10/02)
- File number:3
-

- 101411-58-9
-
Long-acting dihydropyridine calcium antagonists. 6. Structure-activity relationships around 4-(2,3-dichlorophenyl)-3-(ethoxycarbonyl)-2-[(2-hydroxyethoxy) methyl]-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine
-
Journal of Medicinal Chemistry p. 19 - 24
(2007/10/02)
- File number:3
-

- 101411-59-0
-
Long-acting dihydropyridine calcium antagonists. 7. Compounds containing unsaturation in the 2-substituent on the 1,4-dihydropyridine ring
-
European Journal of Medicinal Chemistry p. 619 - 624
(2007/10/02)
- File number:2
-

- 101411-60-3
-
Long-acting dihydropyridine calcium antagonists. 7. Compounds containing unsaturation in the 2-substituent on the 1,4-dihydropyridine ring
-
European Journal of Medicinal Chemistry p. 619 - 624
(2007/10/02)
- File number:2
-

- 101411-61-4
-
Long-acting dihydropyridine calcium antagonists. 6. Structure-activity relationships around 4-(2,3-dichlorophenyl)-3-(ethoxycarbonyl)-2-[(2-hydroxyethoxy) methyl]-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine
-
Journal of Medicinal Chemistry p. 19 - 24
(2007/10/02)
- File number:1
-

- 101411-64-7
-
Long-acting dihydropyridine calcium antagonists. 3. Synthesis and structure-activity relationships for a series of 2-[(heterocyclylmethoxy) methyl]derivatives
-
Journal of Medicinal Chemistry p. 2381 - 2388
(2007/10/02)
- File number:4
-

- 101411-65-8
-
Long-acting dihydropyridine calcium antagonists. 3. Synthesis and structure-activity relationships for a series of 2-[(heterocyclylmethoxy) methyl]derivatives
-
Journal of Medicinal Chemistry p. 2381 - 2388
(2007/10/02)
- File number:4
-

- 101417-38-3
-
The Synthesis of Hallachrome Leucotriacetate (2,7,8-Triacetoxy-1-methoxy-3-methylanthracene)
-
Australian Journal of Chemistry p. 1481 - 1489
(2007/10/02)
- File number:1
-

- 101417-39-4
-
The Synthesis of Hallachrome Leucotriacetate (2,7,8-Triacetoxy-1-methoxy-3-methylanthracene)
-
Australian Journal of Chemistry p. 1481 - 1489
(2007/10/02)
- File number:1
-

- 101417-40-7
-
Structure-Guided Design of EED Binders Allosterically Inhibiting the Epigenetic Polycomb Repressive Complex 2 (PRC2) Methyltransferase
-
Journal of Medicinal Chemistry p. 415 - 427
(2017/04/26)
- File number:6
-

- 101417-41-8
-
The Synthesis of Hallachrome Leucotriacetate (2,7,8-Triacetoxy-1-methoxy-3-methylanthracene)
-
Australian Journal of Chemistry p. 1481 - 1489
(2007/10/02)
- File number:1
-

- 101417-42-9
-
The Synthesis of Hallachrome Leucotriacetate (2,7,8-Triacetoxy-1-methoxy-3-methylanthracene)
-
Australian Journal of Chemistry p. 1481 - 1489
(2007/10/02)
- File number:1
-

- 101417-48-5
-
The Synthesis of Hallachrome Leucotriacetate (2,7,8-Triacetoxy-1-methoxy-3-methylanthracene)
-
Australian Journal of Chemistry p. 1481 - 1489
(2007/10/02)
- File number:1
-

- 101417-69-0
-
PENTAFLUOROETHYLLITHIUM. GENERATION AND USE IN SYNTHESIS
-
Tetrahedron Letters p. 5243 - 5246
(2007/10/02)
- File number:3
-

- 101417-70-3
-
Preparation of Trifluoromethyl and Other Perfluoroalkyl Compounds with (Perfluoroalkyl)trimethylsilanes
-
Journal of Organic Chemistry p. 984 - 989
(2007/10/02)
- File number:4
-

- 101417-71-4
-
Nucleophilic Addition of the Pentafluoroethyl Group to Aldehydes, Ketones, and Esters
-
Journal of Organic Chemistry p. 2481 - 2490
(2007/10/02)
- File number:2
-

- 101417-76-9
-
CHIRAL POOL SYNTHESIS OF TETRALIN AS AB RING SEGMENT, PRECURSOR OF ANTHRACYCLINES.
-
Tetrahedron Letters p. 5295 - 5298
(2007/10/02)
- File number:2
-

- 1014-25-1
-
Synthesis and biological activity of acylthiourea derivatives contain 1,2,3-thiadiazole and 1,3,4-thiadiazole
-
Letters in drug design and discovery p. 314 - 318
(2015/04/14)
- File number:73
-

- 101449-10-9
-
Retinobenzoic Acids. 1. Structure-Activity Relationships of Aromatic Amides with Retinoidal Activity
-
Journal of Medicinal Chemistry p. 2182 - 2192
(2007/10/02)
- File number:2
-

- 101458-87-1
-
Redox-triggered Ci-C coupling of diols and alkynes: Synthesis of β,γ-unsaturated α-hydroxyketones and furans by ruthenium-catalyzed hydrohydroxyalkylation
-
Angewandte Chemie - International Edition p. 3232 - 3235
(2014/04/03)
- File number:4
-

- 10145-97-8
-
Mechanism study on the oligomerization of amino acids into peptides by phosphorus trichloride
-
Phosphorus, Sulfur and Silicon and the Related Elements p. 691 - 698
(2009/05/07)
- File number:1
-

- 101459-81-8
-
Catalytic Z-selective cross-metathesis with secondary silyl- and benzyl-protected allylic ethers: Mechanistic aspects and applications to natural product synthesis
-
Angewandte Chemie - International Edition p. 8395 - 8400
(2013/09/02)
- File number:1
-

- 101460-52-0
-
Potential Antipsychotic Agents. 5. Synthesis and Antidopaminergic Properties of Substituted 5,6-Dimethoxysalicylamides and Related Compounds
-
Journal of Medicinal Chemistry p. 1155 - 1163
(2007/10/02)
- File number:1
-

- 101460-53-1
-
Potential Antipsychotic Agents. 5. Synthesis and Antidopaminergic Properties of Substituted 5,6-Dimethoxysalicylamides and Related Compounds
-
Journal of Medicinal Chemistry p. 1155 - 1163
(2007/10/02)
- File number:2
-

- 101460-54-2
-
Potential antipsychotic agents. 9. Synthesis and stereoselective dopamine D-2 receptor blockade of a potent class of substituted (R)-N-[(1-benzyl-2-pyrrolidinyl)methyl]benzamides. Relations to other side chain congeners
-
Journal of Medicinal Chemistry p. 948 - 955
(2007/10/02)
- File number:1
-

- 101460-57-5
-
Potential Antipsychotic Agents. 5. Synthesis and Antidopaminergic Properties of Substituted 5,6-Dimethoxysalicylamides and Related Compounds
-
Journal of Medicinal Chemistry p. 1155 - 1163
(2007/10/02)
- File number:2
-

- 101460-58-6
-
Potential neuroleptic agents. 4. Chemistry, behavioral pharmacology, and inhibition of [3H]spiperone binding of 3,5-disubstituted N-[(1-ethyl-2-pyrrolidinyl)methyl]-6-methoxysalicylamides
-
Journal of Medicinal Chemistry p. 61 - 69
(2007/10/02)
- File number:1
-

- 101460-64-4
-
Potential Antipsychotic Agents. 5. Synthesis and Antidopaminergic Properties of Substituted 5,6-Dimethoxysalicylamides and Related Compounds
-
Journal of Medicinal Chemistry p. 1155 - 1163
(2007/10/02)
- File number:1
-

- 101460-65-5
-
OXYSALICYLAMIDO DERIVATIVES
-
- File number:1
-

- 101463-46-1
-
Synthesis of α- and γ-(N-carbobenzoxy- and N-tert-butyloxcarbonyl-L-glutamyl)cholines
-
Chemical and Pharmaceutical Bulletin p. 5062 - 5067
(2007/10/02)
- File number:1
-
