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Rational design of RAR-selective ligands revealed by RARβ crystal stucture

EMBO reports, 2004-09, Vol.5 (9), p.877-882

2004

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New azole antagonists with high affinity for the P2Y1 receptor

Bioorganic & medicinal chemistry letters, 2013-06, Vol.23 (12), p.3519-3522

2013

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Synergistic cytotoxicity exhibited by combination treatment of selective retinoid ligands with Taxol (paclitaxel)

Cancer research (Chicago, Ill.), 2001-12, Vol.61 (24), p.8703-8711

2001

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Synthesis and KCNQ2 opener activity of N-(1-benzo[1,3]dioxol-5-yl-ethyl, N-[1-(2,3-dihydro-benzofuran-5-yl)-ethyl, and N-[1-(2,3-dihydro-1 H-indol-5-yl)-ethyl acrylamides

Bioorganic & medicinal chemistry letters, 2004-09, Vol.14 (17), p.4533-4537

2004

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Novel mimics of sialyl Lewis X: design, synthesis and biological activity of a series of 2- and 3-malonate substituted galactoconjugates

Bioorganic & medicinal chemistry, 2001-06, Vol.9 (6), p.1395-1427

2001

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New azole antagonists with high affinity for the P2Y(1) receptor

Bioorganic & medicinal chemistry letters, 2013-06, Vol.23 (12), p.3519-3522

2013

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Five-membered heterocyclic thiones. Part VI. 2-methyl-1,2,3-triazole-4-thiol

Journal of heterocyclic chemistry, 1975-08, Vol.12 (4), p.761-762

1975

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Anhydropenicillin: a key intermediate for the stereocontrolled introduction of the 6-R-hydroxyethyl side chain of the penem and carbapenem antibiotics

Canadian journal of chemistry, 1987-09, Vol.65 (9), p.2179-2181

1987

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Rational design of RAR-selective ligands revealed by RARbeta crystal stucture

EMBO reports, 2004-09, Vol.5 (9), p.877-882

2004

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Rational design of RAR-selective ligands revealed by RAR[beta] crystal stucture

EMBO reports, 2004-09, Vol.5 (9), p.877

2004

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Synthesis and KCNQ2 opener activity of N-1-benzo[1,3]dioxol-5-yl-ethyl, N-[1-(2,3-dihydro-benzofuran-5-yl)-ethyl, and N-[1-(2,3-dihydro-1H-indol-5-yl)-ethyl acrylamides

Bioorganic & medicinal chemistry letters, 2004, Vol.14 (17), p.4533-4537

2004

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Novel mimics of sialyl Lewis X

Bioorganic & medicinal chemistry, 2001-06, Vol.9 (6), p.1395-1427

2001

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2-Picolyl thioesters; a useful synthon for the preparation of 1-β-alkyl carbapenem intermediates

Canadian journal of chemistry, 1988-06, Vol.66 (6), p.1537-1539

1988

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Phenyl group as a probe in the 1 H nuclear magnetic resonance study of the conformations of quaternary heteroaromatic carbapenem antibiotics. Identification of the site of quaternization in -SCH 2 - substituted nitrogen-containing heteroaromatic derivatives

Canadian journal of chemistry, 1988-07, Vol.66 (7), p.1546-1551

1988

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5-Allyl-9-oxobenzomorphans. Part 4. Synthesis of 3-hydroxy-8-oxyisomorphinans, 5-allyl-9α-hydroxy-6,7-benzomorphans, and related tetrahydrofuranobenzomorphans

Canadian journal of chemistry, 1977-07, Vol.55 (13), p.2523-2529

1977

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Nuclear analogs of β-lactam antibiotics. XVII. Stereospecific synthesis of penem and carbapenem precursors

Canadian journal of chemistry, 1983-08, Vol.61 (8), p.1899-1901

1983

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Analgesics and narcotic antagonists in the benzomorphan and 8-oxamorphinan series. 5

Journal of medicinal chemistry, 1978-05, Vol.21 (5), p.423-427

1978

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Nuclear analogs of β-lactam antibiotics. XV. Synthesis of 6-substituted 2-methylpenem-3-carboxylic acids

Canadian journal of chemistry, 1982-04, Vol.60 (7), p.904-909

1982

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Nuclear analogs of β-lactam antibiotics. XVI. Aldol condensations of N-protected 4-tritylthio-2-azetidinones

Canadian journal of chemistry, 1983-03, Vol.61 (3), p.613-618

1983

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5-Allyl-9-oxobenzomorphans. 3. Potent narcotic antagonists and analgesics-antagonists in the series of substituted 2',9.beta.-dihydroxy-6,7-benzomorphans

Journal of medicinal chemistry, 1977-05, Vol.20 (5), p.676-682

1977

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The Photochemical Isomerization of N-Bromo-α,β-unsaturated Lactams; An Intermolecular Allylic Bromination Process Involving a Probable Bromine Radical Chain

Canadian journal of chemistry, 1974-02, Vol.52 (4), p.645-652

1974

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Nuclear analogs of β-lactam antibiotics. XIV. Synthesis of penems via (4-tritylthio-2-azetidinon-1-yl)triphenylphosphoranylideneacetates

Canadian journal of chemistry, 1982-04, Vol.60 (7), p.942-944

1982

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Ring C substituted 14-hydroxymorphinans and isomorphinans as narcotic antagonists

Canadian journal of chemistry, 1976-02, Vol.54 (3), p.429-439

1976

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ChemInform Abstract: RING C SUBSTITUTED 14‐HYDROXYMORPHINANS AND ISOMORPHINANS AS NARCOTIC ANTAGONISTS

Chemischer Informationsdienst, 1976-06, Vol.7 (25)

1976

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ChemInform Abstract: THE PHOTOCHEMICAL ISOMERIZATION OF N‐BROMO‐ALPHA,BETA‐UNSATURATED LACTAMS, AN INTERMOLECULAR ALLYLIC BROMINATION PROCESS INVOLVING A PROBABLE BROMINE RADICAL CHAIN

Chemischer Informationsdienst, 1974-05, Vol.5 (18)

1974

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Rational design of RAR-selective ligands revealed by RARβ crystal stucture

New azole antagonists with high affinity for the P2Y1 receptor

Synergistic cytotoxicity exhibited by combination treatment of selective retinoid ligands with Taxol (paclitaxel)

Synthesis and KCNQ2 opener activity of N-(1-benzo[1,3]dioxol-5-yl-ethyl, N-[1-(2,3-dihydro-benzofuran-5-yl)-ethyl, and N-[1-(2,3-dihydro-1 H-indol-5-yl)-ethyl acrylamides

Novel mimics of sialyl Lewis X: design, synthesis and biological activity of a series of 2- and 3-malonate substituted galactoconjugates

New azole antagonists with high affinity for the P2Y(1) receptor

Five-membered heterocyclic thiones. Part VI. 2-methyl-1,2,3-triazole-4-thiol

Anhydropenicillin: a key intermediate for the stereocontrolled introduction of the 6-R-hydroxyethyl side chain of the penem and carbapenem antibiotics

Rational design of RAR-selective ligands revealed by RARbeta crystal stucture

Rational design of RAR-selective ligands revealed by RAR[beta] crystal stucture

Synthesis and KCNQ2 opener activity of N-1-benzo[1,3]dioxol-5-yl-ethyl, N-[1-(2,3-dihydro-benzofuran-5-yl)-ethyl, and N-[1-(2,3-dihydro-1H-indol-5-yl)-ethyl acrylamides

Novel mimics of sialyl Lewis X

2-Picolyl thioesters; a useful synthon for the preparation of 1-β-alkyl carbapenem intermediates

Phenyl group as a probe in the 1 H nuclear magnetic resonance study of the conformations of quaternary heteroaromatic carbapenem antibiotics. Identification of the site of quaternization in -SCH 2 - substituted nitrogen-containing heteroaromatic derivatives

5-Allyl-9-oxobenzomorphans. Part 4. Synthesis of 3-hydroxy-8-oxyisomorphinans, 5-allyl-9α-hydroxy-6,7-benzomorphans, and related tetrahydrofuranobenzomorphans

Nuclear analogs of β-lactam antibiotics. XVII. Stereospecific synthesis of penem and carbapenem precursors

Analgesics and narcotic antagonists in the benzomorphan and 8-oxamorphinan series. 5

Nuclear analogs of β-lactam antibiotics. XV. Synthesis of 6-substituted 2-methylpenem-3-carboxylic acids

Nuclear analogs of β-lactam antibiotics. XVI. Aldol condensations of N-protected 4-tritylthio-2-azetidinones

5-Allyl-9-oxobenzomorphans. 3. Potent narcotic antagonists and analgesics-antagonists in the series of substituted 2',9.beta.-dihydroxy-6,7-benzomorphans

The Photochemical Isomerization of N-Bromo-α,β-unsaturated Lactams; An Intermolecular Allylic Bromination Process Involving a Probable Bromine Radical Chain

Nuclear analogs of β-lactam antibiotics. XIV. Synthesis of penems via (4-tritylthio-2-azetidinon-1-yl)triphenylphosphoranylideneacetates

Ring C substituted 14-hydroxymorphinans and isomorphinans as narcotic antagonists

ChemInform Abstract: RING C SUBSTITUTED 14‐HYDROXYMORPHINANS AND ISOMORPHINANS AS NARCOTIC ANTAGONISTS

ChemInform Abstract: THE PHOTOCHEMICAL ISOMERIZATION OF N‐BROMO‐ALPHA,BETA‐UNSATURATED LACTAMS, AN INTERMOLECULAR ALLYLIC BROMINATION PROCESS INVOLVING A PROBABLE BROMINE RADICAL CHAIN

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