- 105577-85-3
-
Selective O-allylation of bisphenol A: Toward a chloride-free route for epoxy resins
-
Applied Organometallic Chemistry p. 207 - 211
(2012/04/23)
- File number:1
-

- 105577-86-4
-
Studies on &β-Carbolines: Synthesis of 2-, 3- and 6-Substituted 9H-Pyridoindoles as Tubal Occluding Agents
-
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry p. 757 - 760
(2007/10/02)
- File number:1
-

- 105577-88-6
-
Studies on &β-Carbolines: Synthesis of 2-, 3- and 6-Substituted 9H-Pyridoindoles as Tubal Occluding Agents
-
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry p. 757 - 760
(2007/10/02)
- File number:1
-

- 105577-89-7
-
Studies on &β-Carbolines: Synthesis of 2-, 3- and 6-Substituted 9H-Pyridoindoles as Tubal Occluding Agents
-
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry p. 757 - 760
(2007/10/02)
- File number:1
-

- 105577-90-0
-
Studies on &β-Carbolines: Synthesis of 2-, 3- and 6-Substituted 9H-Pyridoindoles as Tubal Occluding Agents
-
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry p. 757 - 760
(2007/10/02)
- File number:1
-

- 10557-79-6
-
Isomerizable (: E / Z)-alkynyl- O -methyl oximes employing TMSCl-NCS in chlorinative cyclization for the direct synthesis of 4-chloroisoxazoles
-
RSC Advances p. 48666 - 48675
(2016/06/09)
- File number:5
-

- 105578-20-9
-
The regiospecific alkylation of histidine side chains
-
Synthesis p. 1110 - 1113
(2007/10/02)
- File number:1
-

- 10557-82-1
-
Asymmetric catalysis of the carbonyl-amine condensation: Kinetic resolution of primary amines
-
Journal of the American Chemical Society p. 1357 - 1359
(2017/02/10)
- File number:5
-

- 105578-30-1
-
PYRIDONE DERIVATIVES AS NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS
-
- File number:2
-

- 10557-85-4
-
Structure-based design of orally bioavailable 1 h -Pyrrolo[3,2- C ]pyridine inhibitors of mitotic kinase monopolar spindle 1 (MPS1)
-
Journal of Medicinal Chemistry p. 10045 - 10065
(2014/01/17)
- File number:9
-

- 105578-59-4
-
Nucleophilic acyl substitutions of anhydrides with protic nucleophiles catalyzed by amphoteric, oxomolybdenum species
-
Journal of Organic Chemistry p. 1188 - 1197
(2007/10/03)
- File number:6
-

- 10557-86-5
-
The hydrogen deuterium exchange of 3,5 dimethylisoxazoles
-
Bulletin of the Chemical Society of Japan p. 1047 - 1049
(2007/10/04)
- File number:4
-

- 105579-35-9
-
Cardioactive aryloxypropanolamines
-
- File number:2
-

- 1055-79-4
-
Pd(OAc)2-catalyzed carbonylation of amines
-
Journal of Organic Chemistry p. 5951 - 5958
(2007/10/03)
- File number:4
-

- 105579-43-9
-
Synthesis and structure-activity relationships of new (5R,8R,10R)-ergoline derivatives with antihypertensive or dopaminergic activity
-
Chemical and Pharmaceutical Bulletin p. 1463 - 1473
(2007/10/02)
- File number:3
-

- 105579-44-0
-
Synthesis and structure-activity relationships of new (5R,8R,10R)-ergoline derivatives with antihypertensive or dopaminergic activity
-
Chemical and Pharmaceutical Bulletin p. 1463 - 1473
(2007/10/02)
- File number:2
-

- 105579-45-1
-
Synthesis and structure-activity relationships of new (5R,8R,10R)-ergoline derivatives with antihypertensive or dopaminergic activity
-
Chemical and Pharmaceutical Bulletin p. 1463 - 1473
(2007/10/02)
- File number:2
-

- 105579-46-2
-
Synthesis and structure-activity relationships of new (5R,8R,10R)-ergoline derivatives with antihypertensive or dopaminergic activity
-
Chemical and Pharmaceutical Bulletin p. 1463 - 1473
(2007/10/02)
- File number:2
-

- 105579-47-3
-
Synthesis and structure-activity relationships of new (5R,8R,10R)-ergoline derivatives with antihypertensive or dopaminergic activity
-
Chemical and Pharmaceutical Bulletin p. 1463 - 1473
(2007/10/02)
- File number:2
-

- 105579-48-4
-
Synthesis and structure-activity relationships of new (5R,8S,10R)-ergoline derivatives with antihypertensive of dopaminergic activity
-
Chemical and Pharmaceutical Bulletin p. 2042 - 2048
(2007/10/02)
- File number:3
-

- 105579-51-9
-
Synthesis and structure-activity relationships of new (5R,8R,10R)-ergoline derivatives with antihypertensive or dopaminergic activity
-
Chemical and Pharmaceutical Bulletin p. 1463 - 1473
(2007/10/02)
- File number:2
-

- 105579-52-0
-
Synthesis and structure-activity relationships of new (5R,8R,10R)-ergoline derivatives with antihypertensive or dopaminergic activity
-
Chemical and Pharmaceutical Bulletin p. 1463 - 1473
(2007/10/02)
- File number:2
-

- 105579-53-1
-
Synthesis and structure-activity relationships of new (5R,8R,10R)-ergoline derivatives with antihypertensive or dopaminergic activity
-
Chemical and Pharmaceutical Bulletin p. 1463 - 1473
(2007/10/02)
- File number:2
-

- 105579-54-2
-
Synthesis and structure-activity relationships of new (5R,8S,10R)-ergoline derivatives with antihypertensive of dopaminergic activity
-
Chemical and Pharmaceutical Bulletin p. 2042 - 2048
(2007/10/02)
- File number:3
-

- 105579-55-3
-
Synthesis and structure-activity relationships of new (5R,8R,10R)-ergoline derivatives with antihypertensive or dopaminergic activity
-
Chemical and Pharmaceutical Bulletin p. 1463 - 1473
(2007/10/02)
- File number:2
-

- 105579-57-5
-
Synthesis and structure-activity relationships of new (5R,8R,10R)-ergoline derivatives with antihypertensive or dopaminergic activity
-
Chemical and Pharmaceutical Bulletin p. 1463 - 1473
(2007/10/02)
- File number:2
-

- 105580-09-4
-
Synthesis and characterization of novel all-organic liquid crystalline radicals
-
Molecular Crystals and Liquid Crystals p. 213 - 221
(2008/03/18)
- File number:2
-

- 105580-33-4
-
Synthesis and Antifolate Properties of 10-Alkyl-5,10-dideaza Analogues of Methotrexate and Tetrahydrofolic Acid
-
Journal of Medicinal Chemistry p. 673 - 677
(2007/10/02)
- File number:1
-

- 105580-41-4
-
The Conversion of tert-Butyl Esters to Acid Chlorides Using Thionyl Chloride
-
Journal of Organic Chemistry p. 3245 - 3251
(2017/03/23)
- File number:8
-

- 105580-45-8
-
Acyloxymethyl as an activating group in lipase-catalyzed enantioselective hydrolysis. A versatile approach to chiral 4-aryl-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylates
-
Tetrahedron Letters p. 5805 - 5808
(2007/10/02)
- File number:1
-

- 105580-46-9
-
Acyloxymethyl as an activating group in lipase-catalyzed enantioselective hydrolysis. A versatile approach to chiral 4-aryl-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylates
-
Tetrahedron Letters p. 5805 - 5808
(2007/10/02)
- File number:3
-

- 105580-47-0
-
Acyloxymethyl as an activating group in lipase-catalyzed enantioselective hydrolysis. A versatile approach to chiral 4-aryl-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylates
-
Tetrahedron Letters p. 5805 - 5808
(2007/10/02)
- File number:2
-

- 105581-76-8
-
Asymmetric Synthesis of (5R,6S)-6-Acetoxy-5-hexadecanolide, the Major Component of the Oviposition Attractant Pheromone of the Mosquito Culex pipens fatigans, and Two of Its Stereoisomers
-
Journal of Organic Chemistry p. 5353 - 5362
(2007/10/02)
- File number:1
-

- 105581-82-6
-
Alkylative kinetic resolution of vicinal diols under phase-transfer conditions: A chiral ammonium borinate catalysis
-
Chemical Science p. 1231 - 1235
(2018/02/09)
- File number:5
-

- 105581-83-7
-
A Valine-Derived Lithiated 3-Methylthiomethyl-1,3-oxazolidin-2-one for Enantioselective Nucleophilic Hydroxymethylation, Formylation, and Alkoxycarbonylation of Aldehydes
-
Organic Letters p. 1501 - 1504
(2007/10/03)
- File number:5
-

- 105582-16-9
-
Unsaturated ozonides from the ozonolysis of cyclodienes in the presence of carbonyl compounds
-
European Journal of Organic Chemistry p. 3083 - 3087
(2007/10/03)
- File number:1
-

- 105582-31-8
-
Synthesis of (R)- and (S)-1-Aminocyclopropane-1-carboxylic Acids
-
Journal of Organic Chemistry p. 15 - 18
(2007/10/02)
- File number:1
-

- 105582-32-9
-
Synthesis of (R)- and (S)-1-Aminocyclopropane-1-carboxylic Acids
-
Journal of Organic Chemistry p. 15 - 18
(2007/10/02)
- File number:2
-

- 105582-33-0
-
Synthesis of (R)- and (S)-1-Aminocyclopropane-1-carboxylic Acids
-
Journal of Organic Chemistry p. 15 - 18
(2007/10/02)
- File number:1
-

- 10558-25-5
-
Orthogonal Stability and Reactivity of Aryl Germanes Enables Rapid and Selective (Multi)Halogenations
-
Angewandte Chemie - International Edition p. 18717 - 18722
(2020/08/25)
- File number:6
-

- 1055-83-0
-
Rhodium-Catalyzed Cyclization of O,ω-Unsaturated Alkoxyamines: Formation of Oxygen-Containing Heterocycles
-
Angewandte Chemie - International Edition p. 574 - 578
(2018/02/21)
- File number:2
-

- 10558-44-8
-
Pd-catalyzed enantioselective C-H iodination: Asymmetric synthesis of chiral diarylmethylamines
-
Journal of the American Chemical Society p. 16344 - 16347
(2013/12/04)
- File number:9
-

- 10558-45-9
-
Aluminum Metal-Organic Framework-Ligated Single-Site Nickel(II)-Hydride for Heterogeneous Chemoselective Catalysis
-
ACS Catalysis p. 3943 - 3957
(2021/04/12)
- File number:13
-

- 10558-47-1
-
ANTIVIRAL COMPOUNDS AND USES THEREOF
-
- File number:3
-

- 105584-71-2
-
Synthesis and Isolation of Aryl Thioaldehyde S-Oxides
-
Journal of the Chemical Society. Chemical communications p. 964 - 965
(2007/10/02)
- File number:2
-

- 105584-72-3
-
Synthesis and Chemical Behaviour of Thioacylsilanes (Silyl Thioketones). Part 1. Oxidation to S-Oxides, Conversion into Silylated Thiiranes, Silylated Triarylethylenes, and α-Silylated Sulphides
-
Journal of the Chemical Society. Perkin transactions I p. 381 - 386
(2007/10/02)
- File number:1
-

- 105584-74-5
-
Synthesis and Chemical Behaviour of Thioacylsilanes (Silyl Thioketones). Part 1. Oxidation to S-Oxides, Conversion into Silylated Thiiranes, Silylated Triarylethylenes, and α-Silylated Sulphides
-
Journal of the Chemical Society. Perkin transactions I p. 381 - 386
(2007/10/02)
- File number:1
-

- 105584-75-6
-
Synthesis and Chemical Behaviour of Thioacylsilanes (Silyl Thioketones). Part 1. Oxidation to S-Oxides, Conversion into Silylated Thiiranes, Silylated Triarylethylenes, and α-Silylated Sulphides
-
Journal of the Chemical Society. Perkin transactions I p. 381 - 386
(2007/10/02)
- File number:1
-

- 105584-76-7
-
Synthesis and Chemical Behaviour of Thioacylsilanes (Silyl Thioketones). Part 1. Oxidation to S-Oxides, Conversion into Silylated Thiiranes, Silylated Triarylethylenes, and α-Silylated Sulphides
-
Journal of the Chemical Society. Perkin transactions I p. 381 - 386
(2007/10/02)
- File number:1
-

- 105584-77-8
-
Synthesis and Chemical Behaviour of Thioacylsilanes (Silyl Thioketones). Part 1. Oxidation to S-Oxides, Conversion into Silylated Thiiranes, Silylated Triarylethylenes, and α-Silylated Sulphides
-
Journal of the Chemical Society. Perkin transactions I p. 381 - 386
(2007/10/02)
- File number:1
-
