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The issue of residual stresses in additive technologies

MATEC web of conferences, 2023, Vol.376, p.1008

2023

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Diastereoselective Synthesis of 2,3,6-Trisubstituted Piperidines

Journal of organic chemistry, 2009-06, Vol.74 (12), p.4525-4536

2009

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Textbooks in School and Society: An Annotated Bibliography and Guide to Research

1, 2012

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Design and Synthesis of 1-Heteroaryl-3-(1-benzyl-4-piperidinyl)propan-1-one Derivatives as Potent, Selective Acetylcholinesterase Inhibitors

Journal of medicinal chemistry, 1995-03, Vol.38 (7), p.1084-1089

1995

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An initial three-component pharmacophore for specific serotonin-3 receptor ligands

Journal of medicinal chemistry, 1990-10, Vol.33 (10), p.2721-2725

1990

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SYNTHESIS, IN VITRO AND IN VIVO ACTIVITY OF NOVEL 9-DEOXO-9a-AZA-9a-HOMOERYTHROMYCIN A DERIVATIVES; A NEW CLASS OF MACROLIDE ANTIBIOTICS, THE AZALIDES

The Journal of Antibiotics, 1988/08/25, Vol.41(8), pp.1029-1047

1988

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1-Naphthylpiperazine derivatives as potential atypical antipsychotic agents

Journal of medicinal chemistry, 1991-06, Vol.34 (6), p.1860-1866

1991

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Thiazole as a carbonyl bioisostere. A novel class of highly potent and selective 5-HT3 receptor antagonists

Journal of medicinal chemistry, 1990-10, Vol.33 (10), p.2715-2720

1990

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Aromatic thiazole derivatives: structurally novel and selective serotonin-3 receptor antagonists

Journal of medicinal chemistry, 1990-01, Vol.33 (1), p.13-16

1990

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5,7-Dihydro-3-[2-[1-(phenylmethyl)-4-piperidinyl]ethyl]-6H-pyrrolo[3,2-f]-1,2-benzisoxazol-6-one: A Potent and Centrally-Selective Inhibitor of Acetylcholinesterase

Journal of medicinal chemistry, 1995-07, Vol.38 (15), p.2802-2808

1995

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2‐Amino‐4‐methylpyridine as a potent inhibitor of inducible NO synthase activity in vitro and in vivo

British journal of pharmacology, 1996-11, Vol.119 (6), p.1101-1108

1996

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Novel Benzisoxazole Derivatives as Potent and Selective Inhibitors of Acetylcholinesterase

Journal of medicinal chemistry, 1994-08, Vol.37 (17), p.2721-2734

1994

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Synthesis, in vitro binding profile, and CNS penetrability of the highly potent 5-HT3 receptor antagonist [3H]-4-(2-methoxyphenyl)-2-[4(5)-methyl-5(4)-imidazolylmethyl]thiazole

Journal of medicinal chemistry, 1990-11, Vol.33 (11), p.3020-3023

1990

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Selective cleavage of the mycinose sugar from the macrolide antibiotic tylosin: a unique glycosidic scission

Journal of organic chemistry, 1979-06, Vol.44 (12), p.2050-2052

1979

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Macrolide neutral sugar chemistry. Chemical conversion of oleandomycin Y to 3-(2,6-dideoxy-L-.alpha.-allosyl)oleandomycin Y and 3-(2,6-dideoxy-L-.alpha.-galactosyl)oleandomycin Y

Journal of organic chemistry, 1982-11, Vol.47 (24), p.4796-4799

1982

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Macrolide fundamental chemistry: sequential conversion of the 14-membered ring macrolide antibiotic oleandomycin to 12- and 10-membered ring macrocyclic lactone systems

Journal of organic chemistry, 1986-12, Vol.51 (26), p.5397-5400

1986

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Bis annelations via 6-methyl-2-vinylpyridine. Efficient synthesis of dl-D-homoestrone

Journal of the American Chemical Society, 1975-01, Vol.97 (2), p.380-387

1975

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5,7-dihydro-3-[2-[1-(phenylmethyl)-4-piperidinyl]ethyl]-6H- pyrrolo[3,2-f]-1,2-benzisoxazol-6-one: a potent and centrally-selective inhibitor of acetylcholinesterase with an improved margin of safety

Journal of medicinal chemistry, 1995-07, Vol.38 (15), p.2802

1995

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Ring contraction of oleandrose on the macrolide antibiotic oleandomycin with [(methoxycarbonyl)sulfamoyl]triethylammonium hydroxide inner salt

Journal of medicinal chemistry, 1982-07, Vol.25 (7), p.881-884

1982

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Novel Serotonin-3 Receptor Antagonists

Synlett, 1991-04, Vol.1991 (4), p.213-221

1991

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13C-NMR. Spectroscopy of Naturally Occurring Substances. XXXV. Labdanic diterpenes

Helvetica chimica acta, 1975-07, Vol.58 (6), p.1567-1573

1975

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Novel in vitro and in vivo inhibitors of prolyl endopeptidase

Bioorganic & medicinal chemistry letters, 1991, Vol.1 (11), p.585-590

1991

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PART I: A BIS-ANNELATION BY MEANS OF 6-VINYL-2-PICOLINE, THE SYNTHESIS OFD-HOMOESTRONE. PART II: THE ALDOLIZATION OF C(7) SUBSTITUTED 2,6 HEPTANEDIONES

NAGEL, ARTHUR ADAM

1971

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Macrolide antibiotics. Chemistry, biology, and practice

Journal of Pharmaceutical Sciences, 1985, Vol.74 (9), p.1023-1023

Nagel, Arthur A.

1985

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Macrolide antibiotics. Chemistry, biology, and practice. Edited by Satoshi Ōmura. Academic Press, Inc., Orlando, FL 32887. 1984. 635 pp. 16 × 23.5 cm. ISBN 0-12-526450-x. $;89.50

Journal of Pharmaceutical Sciences, 1985, Vol.74 (9), p.1023-1023

Nagel, Arthur A.

1985

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The issue of residual stresses in additive technologies

Diastereoselective Synthesis of 2,3,6-Trisubstituted Piperidines

Textbooks in School and Society: An Annotated Bibliography and Guide to Research

Design and Synthesis of 1-Heteroaryl-3-(1-benzyl-4-piperidinyl)propan-1-one Derivatives as Potent, Selective Acetylcholinesterase Inhibitors

An initial three-component pharmacophore for specific serotonin-3 receptor ligands

SYNTHESIS, IN VITRO AND IN VIVO ACTIVITY OF NOVEL 9-DEOXO-9a-AZA-9a-HOMOERYTHROMYCIN A DERIVATIVES; A NEW CLASS OF MACROLIDE ANTIBIOTICS, THE AZALIDES

1-Naphthylpiperazine derivatives as potential atypical antipsychotic agents

Thiazole as a carbonyl bioisostere. A novel class of highly potent and selective 5-HT3 receptor antagonists

Aromatic thiazole derivatives: structurally novel and selective serotonin-3 receptor antagonists

5,7-Dihydro-3-[2-[1-(phenylmethyl)-4-piperidinyl]ethyl]-6H-pyrrolo[3,2-f]-1,2-benzisoxazol-6-one: A Potent and Centrally-Selective Inhibitor of Acetylcholinesterase

2‐Amino‐4‐methylpyridine as a potent inhibitor of inducible NO synthase activity in vitro and in vivo

Novel Benzisoxazole Derivatives as Potent and Selective Inhibitors of Acetylcholinesterase

Synthesis, in vitro binding profile, and CNS penetrability of the highly potent 5-HT3 receptor antagonist [3H]-4-(2-methoxyphenyl)-2-[4(5)-methyl-5(4)-imidazolylmethyl]thiazole

Selective cleavage of the mycinose sugar from the macrolide antibiotic tylosin: a unique glycosidic scission

Macrolide neutral sugar chemistry. Chemical conversion of oleandomycin Y to 3-(2,6-dideoxy-L-.alpha.-allosyl)oleandomycin Y and 3-(2,6-dideoxy-L-.alpha.-galactosyl)oleandomycin Y

Macrolide fundamental chemistry: sequential conversion of the 14-membered ring macrolide antibiotic oleandomycin to 12- and 10-membered ring macrocyclic lactone systems

Bis annelations via 6-methyl-2-vinylpyridine. Efficient synthesis of dl-D-homoestrone

5,7-dihydro-3-[2-[1-(phenylmethyl)-4-piperidinyl]ethyl]-6H- pyrrolo[3,2-f]-1,2-benzisoxazol-6-one: a potent and centrally-selective inhibitor of acetylcholinesterase with an improved margin of safety

Ring contraction of oleandrose on the macrolide antibiotic oleandomycin with [(methoxycarbonyl)sulfamoyl]triethylammonium hydroxide inner salt

Novel Serotonin-3 Receptor Antagonists

13C-NMR. Spectroscopy of Naturally Occurring Substances. XXXV. Labdanic diterpenes

Novel in vitro and in vivo inhibitors of prolyl endopeptidase

PART I: A BIS-ANNELATION BY MEANS OF 6-VINYL-2-PICOLINE, THE SYNTHESIS OFD-HOMOESTRONE. PART II: THE ALDOLIZATION OF C(7) SUBSTITUTED 2,6 HEPTANEDIONES

Macrolide antibiotics. Chemistry, biology, and practice

Macrolide antibiotics. Chemistry, biology, and practice. Edited by Satoshi Ōmura. Academic Press, Inc., Orlando, FL 32887. 1984. 635 pp. 16 × 23.5 cm. ISBN 0-12-526450-x. $;89.50

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