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Synthesis of 4′-Thionucleosides as Antitumor and Antiviral Agents

Chemical and Pharmaceutical Bulletin, 2018/02/01, Vol.66(2), pp.139-146

2018

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Palladium-Catalyzed Three-Component Coupling of Ynamides

Organic letters, 2020-07, Vol.22 (14), p.5299-5303

2020

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Glycosylation reactions mediated by hypervalent iodine: application to the synthesis of nucleosides and carbohydrates

Beilstein journal of organic chemistry, 2018-06, Vol.14 (1), p.1595-1618

2018

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Gabapentin Inhibits Bortezomib-Induced Mechanical Allodynia Through Supraspinal Action in Mice

Journal of Pharmacological Sciences, 2014/04/20, Vol.124(4), pp.502-510

2014

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Asymmetric synthesis of 2,5-disubstituted 3-hydroxypyrrolidines based on stereodivergent intramolecular iridium-catalyzed allylic aminations

Organic & biomolecular chemistry, 2014-03, Vol.12 (12), p.1983-1994

2014

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A facile synthesis of fully protected meso-diaminopimelic acid (DAP) and its application to the preparation of lipophilic N-acyl iE-DAP

Molecules (Basel, Switzerland), 2013-01, Vol.18 (1), p.1162-1173

2013

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A mouse model of peripheral postischemic dysesthesia: involvement of reperfusion-induced oxidative stress and TRPA1 channel

The Journal of pharmacology and experimental therapeutics, 2014-12, Vol.351 (3), p.568

2014

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Synthesis of 1-(5,6-dihydro-2 H-thiopyran-2-yl)uracil by a Pummerer-type thioglycosylation reaction: the regioselectivity of allylic substitution

Tetrahedron, 2009-11, Vol.65 (45), p.9091-9102

2009

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A novel tert-butoxycarbonylation reagent: 1- tert-butoxy-2- tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI)

Tetrahedron, 2006-12, Vol.62 (50), p.11599-11607

2006

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Chemoselective O- tert-butoxycarbonylation of phenols using 6,7-dimethoxyisoquinoline as a novel organocatalyst

Tetrahedron letters, 2010-12, Vol.51 (52), p.6915-6917

2010

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Synthesis of 5-thiodidehydropyranylcytosine derivatives as potential anti-HIV agents

Bioorganic & medicinal chemistry letters, 2011-06, Vol.21 (11), p.3313-3316

2011

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Practical Synthesis of 4′‐Thioribonucleosides from L ‐Arabinose via Novel Reductive Ring‐Contraction Reaction and Pummerer‐Type Thioglycosylation

Current Protocols in Nucleic Acid Chemistry, 2017-12, Vol.71 (1)

2017

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A straightforward stereoselective synthesis of meso-, ( S, S)- and ( R, R)-2,6-diaminopimelic acids from cis-1,4-diacetoxycyclohept-2-ene

Bioorganic & medicinal chemistry letters, 2007-11, Vol.17 (21), p.5894-5896

2007

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1-tert-Butoxy-2-tert-butoxycarbonyl- 1,2-dihydroisoquinoline: A Novel and Chemoselective tert-Butoxycarbonylation Reagent

Organic letters, 2002-02, Vol.4 (4), p.585-587

2002

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An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation

Beilstein journal of organic chemistry, 2007-10, Vol.3 (1), p.37-37

2007

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Carboxamidation of carboxylic acids with 1- tert-butoxy-2- tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI) without bases

Tetrahedron, 2008-12, Vol.64 (49), p.11129-11135

2008

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Synthesis of both enantiomers of hydroxypipecolic acid derivatives equivalent to 5-azapyranuronic acids and evaluation of their inhibitory activities against glycosidases

Bioorganic & medicinal chemistry, 2008-09, Vol.16 (17), p.8273-8286

2008

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A new route to trans-2,6-disubstituted piperidine-related alkaloids using a novel C2-symmetric 2,6-diallylpiperidine carboxylic acid methyl ester

Organic & biomolecular chemistry, 2006-04, Vol.4 (8), p.1587-1595

2006

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Asymmetric synthesis of 2,5-disubstituted 3-hydroxypyrrolidines based on stereodivergent intramolecular iridium-catalyzed allylic aminationsElectronic supplementary information (ESI) available. See DOI: 10.1039/c3ob42229a

2014-02

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A novel 1-tert-butoxy-2-tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI)-catalyzed esterification of N-protected amino acids with nearly equimolar amounts of alcohols in the presence of Boc2O

Tetrahedron letters, 2006-05, Vol.47 (18), p.3099-3102

2006

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A novel 1- tert-butoxy-2- tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI)-catalyzed esterification of N-protected amino acids with nearly equimolar amounts of alcohols in the presence of Boc 2O

Tetrahedron letters, 2006, Vol.47 (18), p.3099-3102

2006

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Diabetic Nephropathy in KK and KK-Ay Mice

Experimental Animals, 2002, Vol.51(2), pp.191-196

2002

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Catalytic Asymmetric Synthesis of Both Enantiomers of Pyrrolizidines 223H’, 239K’, 265H’, and 267H’ Found in Madagascan Frogs (Mantella) and Their Affinities for Nicotinic Acetylcholine Receptor

Heterocycles, 2009, Vol.79 (1), p.1043

2009

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Simple and mild esterification of N-protected amino acids with nearly equimolar amounts of alcohols using 1- tert-butoxy-2- tert-butoxycarbonyl-1,2-dihydroisoquinoline

Tetrahedron letters, 2005-02, Vol.46 (8), p.1277-1279

2005

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Increase in plasma fibrinogen and plasminogen activator inhibitor level in diabetic KK and KK-Ay mice

In vivo (Athens), 2003-01, Vol.17 (1), p.5

2003

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Synthesis of 4′-Thionucleosides as Antitumor and Antiviral Agents

Palladium-Catalyzed Three-Component Coupling of Ynamides

Glycosylation reactions mediated by hypervalent iodine: application to the synthesis of nucleosides and carbohydrates

Gabapentin Inhibits Bortezomib-Induced Mechanical Allodynia Through Supraspinal Action in Mice

Asymmetric synthesis of 2,5-disubstituted 3-hydroxypyrrolidines based on stereodivergent intramolecular iridium-catalyzed allylic aminations

A facile synthesis of fully protected meso-diaminopimelic acid (DAP) and its application to the preparation of lipophilic N-acyl iE-DAP

A mouse model of peripheral postischemic dysesthesia: involvement of reperfusion-induced oxidative stress and TRPA1 channel

Synthesis of 1-(5,6-dihydro-2 H-thiopyran-2-yl)uracil by a Pummerer-type thioglycosylation reaction: the regioselectivity of allylic substitution

A novel tert-butoxycarbonylation reagent: 1- tert-butoxy-2- tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI)

Chemoselective O- tert-butoxycarbonylation of phenols using 6,7-dimethoxyisoquinoline as a novel organocatalyst

Synthesis of 5-thiodidehydropyranylcytosine derivatives as potential anti-HIV agents

Practical Synthesis of 4′‐Thioribonucleosides from L ‐Arabinose via Novel Reductive Ring‐Contraction Reaction and Pummerer‐Type Thioglycosylation

A straightforward stereoselective synthesis of meso-, ( S, S)- and ( R, R)-2,6-diaminopimelic acids from cis-1,4-diacetoxycyclohept-2-ene

1-tert-Butoxy-2-tert-butoxycarbonyl- 1,2-dihydroisoquinoline: A Novel and Chemoselective tert-Butoxycarbonylation Reagent

An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation

Carboxamidation of carboxylic acids with 1- tert-butoxy-2- tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI) without bases

Synthesis of both enantiomers of hydroxypipecolic acid derivatives equivalent to 5-azapyranuronic acids and evaluation of their inhibitory activities against glycosidases

A new route to trans-2,6-disubstituted piperidine-related alkaloids using a novel C2-symmetric 2,6-diallylpiperidine carboxylic acid methyl ester

Asymmetric synthesis of 2,5-disubstituted 3-hydroxypyrrolidines based on stereodivergent intramolecular iridium-catalyzed allylic aminationsElectronic supplementary information (ESI) available. See DOI: 10.1039/c3ob42229a

A novel 1-tert-butoxy-2-tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI)-catalyzed esterification of N-protected amino acids with nearly equimolar amounts of alcohols in the presence of Boc2O

A novel 1- tert-butoxy-2- tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI)-catalyzed esterification of N-protected amino acids with nearly equimolar amounts of alcohols in the presence of Boc 2O

Diabetic Nephropathy in KK and KK-Ay Mice

Catalytic Asymmetric Synthesis of Both Enantiomers of Pyrrolizidines 223H’, 239K’, 265H’, and 267H’ Found in Madagascan Frogs (Mantella) and Their Affinities for Nicotinic Acetylcholine Receptor

Simple and mild esterification of N-protected amino acids with nearly equimolar amounts of alcohols using 1- tert-butoxy-2- tert-butoxycarbonyl-1,2-dihydroisoquinoline

Increase in plasma fibrinogen and plasminogen activator inhibitor level in diabetic KK and KK-Ay mice

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