- 100448-56-4
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Synthesis, Saludiuretic, and Antihypertensive Activity of 6,7-Disubstituted 1(2H)- and 3,4-Dihydro-1(2H)-phthalazinones
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Journal of Medicinal Chemistry p. 947 - 959
(2007/10/02)
- File number:1
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- 100448-58-6
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Synthesis, Saludiuretic, and Antihypertensive Activity of 6,7-Disubstituted 1(2H)- and 3,4-Dihydro-1(2H)-phthalazinones
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Journal of Medicinal Chemistry p. 947 - 959
(2007/10/02)
- File number:1
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- 1004-52-0
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Asymmetric synthesis of tanshindiol A
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Journal of Organic Chemistry p. 5301 - 5312
(2007/10/02)
- File number:6
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- 100460-09-1
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NUCLEOPHILIC RING CLEAVAGE OF CROWN ETHERS, NOVEL METHOD FOR BUILDING UP CROWN ETHER RINGS
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Tetrahedron Letters p. 2705 - 2708
(2007/10/02)
- File number:2
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- 100460-10-4
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NUCLEOPHILIC RING CLEAVAGE OF CROWN ETHERS, NOVEL METHOD FOR BUILDING UP CROWN ETHER RINGS
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Tetrahedron Letters p. 2705 - 2708
(2007/10/02)
- File number:1
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- 100460-17-1
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A facile synthesis of 3-(1-benzyloxymethyl-3-hydroxypropyl)-2,5-piperazinedione
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Bulletin of the Chemical Society of Japan p. 1845 - 1846
(2007/10/02)
- File number:1
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- 100460-62-6
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THIA-ACYLIMINIUM CYCLISATIONS. SYNTHESIS OF FIVE-MEMBERED RINGS AND MACROCYCLES
-
Tetrahedron p. 1999 - 2006
(2007/10/02)
- File number:1
-
- 100460-63-7
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THIA-ACYLIMINIUM CYCLISATIONS. SYNTHESIS OF FIVE-MEMBERED RINGS AND MACROCYCLES
-
Tetrahedron p. 1999 - 2006
(2007/10/02)
- File number:1
-
- 100460-64-8
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THIA-ACYLIMINIUM CYCLISATIONS. SYNTHESIS OF FIVE-MEMBERED RINGS AND MACROCYCLES
-
Tetrahedron p. 1999 - 2006
(2007/10/02)
- File number:1
-
- 100460-65-9
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THIA-ACYLIMINIUM CYCLISATIONS. SYNTHESIS OF FIVE-MEMBERED RINGS AND MACROCYCLES
-
Tetrahedron p. 1999 - 2006
(2007/10/02)
- File number:1
-
- 100460-66-0
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THIA-ACYLIMINIUM CYCLISATIONS. SYNTHESIS OF FIVE-MEMBERED RINGS AND MACROCYCLES
-
Tetrahedron p. 1999 - 2006
(2007/10/02)
- File number:1
-
- 100460-68-2
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COPPER(II) IN ORGANIC SYNTHESIS. IV REACTION OF THE COPPER(II) ACETATE COMPLEX OF ISATIN-3-ARYLHYDRAZONES WITH DIMETHYL ACETYLENEDICARBOXYLATE.
-
Tetrahedron p. 2545 - 2556
(2007/10/02)
- File number:1
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- 100466-49-7
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An asymmetric synthesis of (+)-morphinans in high enantiomeric purity
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Journal of Organic Chemistry p. 872 - 875
(2007/10/02)
- File number:1
-
- 100466-50-0
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An asymmetric synthesis of (+)-morphinans in high enantiomeric purity
-
Journal of Organic Chemistry p. 872 - 875
(2007/10/02)
- File number:1
-
- 100466-51-1
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An asymmetric synthesis of (+)-morphinans in high enantiomeric purity
-
Journal of Organic Chemistry p. 872 - 875
(2007/10/02)
- File number:1
-
- 100466-52-2
-
An asymmetric synthesis of (+)-morphinans in high enantiomeric purity
-
Journal of Organic Chemistry p. 872 - 875
(2007/10/02)
- File number:1
-
- 100466-53-3
-
An asymmetric synthesis of (+)-morphinans in high enantiomeric purity
-
Journal of Organic Chemistry p. 872 - 875
(2007/10/02)
- File number:1
-
- 100466-54-4
-
An asymmetric synthesis of (+)-morphinans in high enantiomeric purity
-
Journal of Organic Chemistry p. 872 - 875
(2007/10/02)
- File number:1
-
- 100466-55-5
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Absolute Configuration of (-)-5-Benzoyl-1,2-dihydro-3H-pyrroloa>pyrrole-1-carboxylic Acid, the Active Enantiomer of Ketorolac
-
Journal of Medicinal Chemistry p. 589 - 591
(2007/10/02)
- File number:1
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- 100466-58-8
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Ester Cleavage by a Phenolic Quaternary Phosphonium Surfactant
-
Journal of Organic Chemistry p. 1352 - 1354
(2007/10/02)
- File number:1
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- 100466-59-9
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Ester Cleavage by a Phenolic Quaternary Phosphonium Surfactant
-
Journal of Organic Chemistry p. 1352 - 1354
(2007/10/02)
- File number:1
-
- 1004-66-6
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FLUORIDE SALTS ON ALUMINA AS REAGENTS FOR ALKYLATION OF PHENOLS AND ALCOHOLS.
-
Bulletin of the Chemical Society of Japan p. 2504 - 2507
(2007/10/02)
- File number:48
-
- 100467-71-8
-
Thromboxane synthetase inhibitors and antihypertensive agents. 1. N-[(1H-imidazol-1-yl)alkyl]aryl amides and N-[(1H-1,2,4-triazol-1-yl)alkyl]aryl amides
-
Journal of Medicinal Chemistry p. 523 - 530
(2007/10/02)
- File number:1
-
- 100467-72-9
-
Thromboxane synthetase inhibitors and antihypertensive agents. 1. N-[(1H-imidazol-1-yl)alkyl]aryl amides and N-[(1H-1,2,4-triazol-1-yl)alkyl]aryl amides
-
Journal of Medicinal Chemistry p. 523 - 530
(2007/10/02)
- File number:1
-
- 100467-74-1
-
Thromboxane synthetase inhibitors and antihypertensive agents. 1. N-[(1H-imidazol-1-yl)alkyl]aryl amides and N-[(1H-1,2,4-triazol-1-yl)alkyl]aryl amides
-
Journal of Medicinal Chemistry p. 523 - 530
(2007/10/02)
- File number:1
-
- 100467-75-2
-
Thromboxane synthetase inhibitors and antihypertensive agents. 1. N-[(1H-imidazol-1-yl)alkyl]aryl amides and N-[(1H-1,2,4-triazol-1-yl)alkyl]aryl amides
-
Journal of Medicinal Chemistry p. 523 - 530
(2007/10/02)
- File number:1
-
- 100467-76-3
-
Thromboxane synthetase inhibitors and antihypertensive agents. 1. N-[(1H-imidazol-1-yl)alkyl]aryl amides and N-[(1H-1,2,4-triazol-1-yl)alkyl]aryl amides
-
Journal of Medicinal Chemistry p. 523 - 530
(2007/10/02)
- File number:1
-
- 100467-78-5
-
Thromboxane synthetase inhibitors and antihypertensive agents. 1. N-[(1H-imidazol-1-yl)alkyl]aryl amides and N-[(1H-1,2,4-triazol-1-yl)alkyl]aryl amides
-
Journal of Medicinal Chemistry p. 523 - 530
(2007/10/02)
- File number:1
-
- 100467-80-9
-
Thromboxane synthetase inhibitors and antihypertensive agents. 1. N-[(1H-imidazol-1-yl)alkyl]aryl amides and N-[(1H-1,2,4-triazol-1-yl)alkyl]aryl amides
-
Journal of Medicinal Chemistry p. 523 - 530
(2007/10/02)
- File number:1
-
- 100467-81-0
-
Thromboxane synthetase inhibitors and antihypertensive agents. 1. N-[(1H-imidazol-1-yl)alkyl]aryl amides and N-[(1H-1,2,4-triazol-1-yl)alkyl]aryl amides
-
Journal of Medicinal Chemistry p. 523 - 530
(2007/10/02)
- File number:1
-
- 100467-82-1
-
Thromboxane synthetase inhibitors and antihypertensive agents. 1. N-[(1H-imidazol-1-yl)alkyl]aryl amides and N-[(1H-1,2,4-triazol-1-yl)alkyl]aryl amides
-
Journal of Medicinal Chemistry p. 523 - 530
(2007/10/02)
- File number:2
-
- 100475-03-4
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Synthesis and aldose reductase-inhibitory activities of structural analogues of WF-3681, a novel aldose reductase inhibitor
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Chemical and Pharmaceutical Bulletin p. 1404 - 1414
(2007/10/02)
- File number:1
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- 100475-04-5
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Synthesis and aldose reductase-inhibitory activities of structural analogues of WF-3681, a novel aldose reductase inhibitor
-
Chemical and Pharmaceutical Bulletin p. 1404 - 1414
(2007/10/02)
- File number:1
-
- 100475-97-6
-
Dialkyl Ether Formation by Nickel-Catalyzed Cross-Coupling of Acetals and Aryl Iodides
-
Angewandte Chemie - International Edition p. 9876 - 9880
(2015/08/19)
- File number:2
-
- 100483-39-4
-
DL-p-methylsulfonylphenyl serine ethyl ester preparation method
-
- File number:4
-
- 1004-83-7
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Oxidative C-arylation of free (NH)-heterocycles via direct (sp3) C-H bond functionalization
-
Journal of the American Chemical Society p. 13244 - 13246
(2007/10/03)
- File number:1
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- 100483-71-4
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Synthesis of β-hydroxy ketones and vinylsilanes from homopropargylic alcohols by intramolecular hydrosilation
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Organic Letters p. 2173 - 2175
(2007/10/03)
- File number:7
-
- 100483-74-7
-
-WITTIG SIGMATROPIC REARRANGEMENT OF CROTYL PROPARGYL ETHER SYSTEM; AN EMERGING TOOL FOR CONTROL OF ACYCLIC STEREOCHEMISTRY
-
Tetrahedron p. 2303 - 2308
(2007/10/02)
- File number:8
-
- 100483-82-7
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THE MECHANISM OF THE HANTZSCH PYRIDINE SYNTHESIS: A STUDY BY 15N AND 13C NMR SPECTROSCOPY
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Tetrahedron p. 5729 - 5738
(2007/10/02)
- File number:9
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- 100486-18-8
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Analogues of Poison Ivy Urushiol. Synthesis and Biological Activity of Disubstituted n-Alkylbenzenes
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Journal of Medicinal Chemistry p. 606 - 611
(2007/10/02)
- File number:1
-
- 100486-19-9
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Analogues of Poison Ivy Urushiol. Synthesis and Biological Activity of Disubstituted n-Alkylbenzenes
-
Journal of Medicinal Chemistry p. 606 - 611
(2007/10/02)
- File number:1
-
- 100486-20-2
-
Analogues of Poison Ivy Urushiol. Synthesis and Biological Activity of Disubstituted n-Alkylbenzenes
-
Journal of Medicinal Chemistry p. 606 - 611
(2007/10/02)
- File number:1
-
- 100486-21-3
-
Analogues of Poison Ivy Urushiol. Synthesis and Biological Activity of Disubstituted n-Alkylbenzenes
-
Journal of Medicinal Chemistry p. 606 - 611
(2007/10/02)
- File number:1
-
- 100486-22-4
-
Analogues of Poison Ivy Urushiol. Synthesis and Biological Activity of Disubstituted n-Alkylbenzenes
-
Journal of Medicinal Chemistry p. 606 - 611
(2007/10/02)
- File number:1
-
- 100486-24-6
-
Analogues of Poison Ivy Urushiol. Synthesis and Biological Activity of Disubstituted n-Alkylbenzenes
-
Journal of Medicinal Chemistry p. 606 - 611
(2007/10/02)
- File number:2
-
- 100486-25-7
-
Analogues of Poison Ivy Urushiol. Synthesis and Biological Activity of Disubstituted n-Alkylbenzenes
-
Journal of Medicinal Chemistry p. 606 - 611
(2007/10/02)
- File number:1
-
- 100486-26-8
-
Analogues of Poison Ivy Urushiol. Synthesis and Biological Activity of Disubstituted n-Alkylbenzenes
-
Journal of Medicinal Chemistry p. 606 - 611
(2007/10/02)
- File number:2
-
- 100486-27-9
-
Analogues of Poison Ivy Urushiol. Synthesis and Biological Activity of Disubstituted n-Alkylbenzenes
-
Journal of Medicinal Chemistry p. 606 - 611
(2007/10/02)
- File number:2
-
- 100486-33-7
-
Angiotensin-converting enzyme inhibitors: New orally active 1,4-thiazepine-2,5-diones, 1,4-thiazine-2,5-diones, and 1,4-benzothiazepine-2,5-diones possessing antihypertensive activity
-
Journal of Medicinal Chemistry p. 784 - 796
(2007/10/02)
- File number:1
-
- 100486-37-1
-
Angiotensin-converting enzyme inhibitors: New orally active 1,4-thiazepine-2,5-diones, 1,4-thiazine-2,5-diones, and 1,4-benzothiazepine-2,5-diones possessing antihypertensive activity
-
Journal of Medicinal Chemistry p. 784 - 796
(2007/10/02)
- File number:1
-
