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Pyrazolopyrimidine nucleosides. 12. Synthesis and biological activity of certain pyrazolo[3,4-d]pyrimidine nucleosides related to adenosine

Journal of medicinal chemistry, 1981-10, Vol.24 (10), p.1165-1172

1981

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Pyrazolopyrimidine nucleosides. Part VIII The synthesis of certain 4-substituted pyrazolo[3,4-d]pyrimidine nucleosides

Journal of heterocyclic chemistry, 1977-05, Vol.14 (3), p.483-487

1977

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THE CHEMISTRY AND BIOLOGICAL ACTIVITY OF CERTAIN 4-SUBSTITUTED AND 3,4-DISUBSTITUTED PYRAZOLO (3,4-d)PYRIMIDINE NUCLEOSIDES

Chemistry and Biology of Nucleosides and Nucleotides, 1978, p.121-134

1978

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Carbonic anhydrase inhibitors: Novel sulfonamides incorporating 1,3,5-triazine moieties as inhibitors of the cytosolic and tumour-associated carbonic anhydrase isozymes I, II and IX

Bioorganic & medicinal chemistry letters, 2005-06, Vol.15 (12), p.3102-3108

2005

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Carbonic anhydrase inhibitors: Synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating 1,2,4-triazine moieties

Bioorganic & medicinal chemistry letters, 2004-11, Vol.14 (21), p.5427-5433

2004

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Embolization of the middle meningeal artery for the prevention of chronic subdural hematoma recurrence in high-risk patients: a randomized controlled trial—the EMPROTECT study protocol

Journal of neurointerventional surgery, 2024-02, p.jnis-2023-021249-2023-021249

2024

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N-(tert-Butoxycarbonyl)-N-[4- (dimethylazaniumylidene)-1,4- dihydropyridin-1-ylsulfonyl]azanide: A New Sulfamoylating Agent. Structure and Reactivity toward Amines

Organic letters, 2001-07, Vol.3 (14), p.2241-2243

2001

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Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating thioureido-sulfanilyl scaffolds

Bioorganic & medicinal chemistry letters, 2005-05, Vol.15 (9), p.2359-2364

2005

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Synthesis of 1,2,5-Thiadiazolidines 1,1-dioxides ( Cyclosulfamides) Starting from Amino Acids and Chlorosulfonyl Isocyanate

Tetrahedron, 2000-01, Vol.56 (3), p.381-387

2000

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Sulfahydantoins as Tripeptide Constraints: Synthesis and Structure of Chiral Substituted 3-Oxo-1,2,5-thiadiazolidine 1,1-Dioxides

European journal of organic chemistry, 1999-09, Vol.1999 (9), p.2275-2283

1999

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Synthesis and in vitro evaluation of S-acyl-3-thiopropyl prodrugs of Foscarnet

Bioorganic & medicinal chemistry, 2004-03, Vol.12 (6), p.1393-1402

2004

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Synthesis of N-Phosphorylsulfamates (as Pyrophosphate and Carbamylphosphate Analogues) through an Imidate-Amidate Rearrangement

Synlett, 2000, Vol.2000 (5), p.0716-0718

2000

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Synthesis of pseudonucleosides containing chiral sulfahydantoins as aglycone (II)

Tetrahedron, 1996-01, Vol.52 (3), p.993-1004

1996

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SYNTHESIS OF 2-CHLOROETHYLNITROSOSULFAMIDES (CENS) VIA A TRANSSULFAMOYLATION REACTION

Phosphorus, sulfur, and silicon and the related elements, 1996-11, Vol.118 (1), p.39-47

1996

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A new family of potential oncostatics: 2-chloroethylnitrososulfamides (CENS)—I. Synthesis, structure, and pharmacological evaluation (preliminary results)

Bioorganic & medicinal chemistry, 1996-08, Vol.4 (8), p.1227-1235

1996

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Expedient synthesis of 2-chloroethylnitrososulfamides (CENS) via the decarboxylative reopening of sulfamoyloxazolidinones

Tetrahedron letters, 1996-08, Vol.37 (32), p.5695-5698

1996

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Simple and efficient synthesis of new chiral N,N′-sulfonyl bis-oxazolidin-2-ones

Heteroatom chemistry, 2006, Vol.17 (1), p.61-65

2006

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3′-C-phosphonates as nucleotides analogues synthesis starting from original C-phosphonosugars (in ribo- and deoxyribo- series)

Tetrahedron, 1994, Vol.50 (28), p.8427-8444

1994

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Sulfonyl bis-N-oxazolidinone (SBO): A new versatile dielectrophile with sequential reactivity

Tetrahedron letters, 1997-12, Vol.38 (50), p.8691-8694

1997

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N-(tert-Butoxycarbonyl)-N-[4-(dimethylazaniumylidene)-1,4-dihydropyridin-1-ylsulfonyl] Azanide: A New Sulfamoylating Agent. Structure and Reactivity toward Amines

Organic letters, 2001-09, Vol.3 (18), p.2939-2939

2001

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N-hydroxysulfamides as analog of N-hydroxyurea: synthesis and biological evaluation

Heteroatom chemistry, 2001, Vol.12 (1), p.1-5

2001

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Direct Synthesis of Z, Boc, Fmoc, Alloc[ddot] Derivatives of 5-Aminooxazoles Starting from Acylamino Acids and Chlorosulfonylcarbamates

Synthetic communications, 2000-07, Vol.30 (14), p.2541-2548

2000

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Galactorrhoea, hyperprolactinaemia, and protease inhibitors

The Lancet (British edition), 2001-02, Vol.357 (9254), p.473-474

2001

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Synthesis of phosphonate analogues of retinyl phosphate

Bioorganic & medicinal chemistry letters, 1995-11, Vol.5 (21), p.2461-2464

1995

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Selective synthesis of sulfonylureas and carboxysulfamides a novel route to oxazolidinones

Tetrahedron letters, 1983, Vol.24 (30), p.3091-3094

1983

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Pyrazolopyrimidine nucleosides. 12. Synthesis and biological activity of certain pyrazolo[3,4-d]pyrimidine nucleosides related to adenosine

Pyrazolopyrimidine nucleosides. Part VIII The synthesis of certain 4-substituted pyrazolo[3,4-d]pyrimidine nucleosides

THE CHEMISTRY AND BIOLOGICAL ACTIVITY OF CERTAIN 4-SUBSTITUTED AND 3,4-DISUBSTITUTED PYRAZOLO (3,4-d)PYRIMIDINE NUCLEOSIDES

Carbonic anhydrase inhibitors: Novel sulfonamides incorporating 1,3,5-triazine moieties as inhibitors of the cytosolic and tumour-associated carbonic anhydrase isozymes I, II and IX

Carbonic anhydrase inhibitors: Synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating 1,2,4-triazine moieties

Embolization of the middle meningeal artery for the prevention of chronic subdural hematoma recurrence in high-risk patients: a randomized controlled trial—the EMPROTECT study protocol

N-(tert-Butoxycarbonyl)-N-[4- (dimethylazaniumylidene)-1,4- dihydropyridin-1-ylsulfonyl]azanide: A New Sulfamoylating Agent. Structure and Reactivity toward Amines

Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating thioureido-sulfanilyl scaffolds

Synthesis of 1,2,5-Thiadiazolidines 1,1-dioxides ( Cyclosulfamides) Starting from Amino Acids and Chlorosulfonyl Isocyanate

Sulfahydantoins as Tripeptide Constraints: Synthesis and Structure of Chiral Substituted 3-Oxo-1,2,5-thiadiazolidine 1,1-Dioxides

Synthesis and in vitro evaluation of S-acyl-3-thiopropyl prodrugs of Foscarnet

Synthesis of N-Phosphorylsulfamates (as Pyrophosphate and Carbamylphosphate Analogues) through an Imidate-Amidate Rearrangement

Synthesis of pseudonucleosides containing chiral sulfahydantoins as aglycone (II)

SYNTHESIS OF 2-CHLOROETHYLNITROSOSULFAMIDES (CENS) VIA A TRANSSULFAMOYLATION REACTION

A new family of potential oncostatics: 2-chloroethylnitrososulfamides (CENS)—I. Synthesis, structure, and pharmacological evaluation (preliminary results)

Expedient synthesis of 2-chloroethylnitrososulfamides (CENS) via the decarboxylative reopening of sulfamoyloxazolidinones

Simple and efficient synthesis of new chiral N,N′-sulfonyl bis-oxazolidin-2-ones

3′-C-phosphonates as nucleotides analogues synthesis starting from original C-phosphonosugars (in ribo- and deoxyribo- series)

Sulfonyl bis-N-oxazolidinone (SBO): A new versatile dielectrophile with sequential reactivity

N-(tert-Butoxycarbonyl)-N-[4-(dimethylazaniumylidene)-1,4-dihydropyridin-1-ylsulfonyl] Azanide: A New Sulfamoylating Agent. Structure and Reactivity toward Amines

N-hydroxysulfamides as analog of N-hydroxyurea: synthesis and biological evaluation

Direct Synthesis of Z, Boc, Fmoc, Alloc[ddot] Derivatives of 5-Aminooxazoles Starting from Acylamino Acids and Chlorosulfonylcarbamates

Galactorrhoea, hyperprolactinaemia, and protease inhibitors

Synthesis of phosphonate analogues of retinyl phosphate

Selective synthesis of sulfonylureas and carboxysulfamides a novel route to oxazolidinones

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