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Physicochemical Parameters and Bioactive Compounds of Strawberry Tree (Arbutus unedo L.) Honey

Journal of chemistry, 2015-01, Vol.2015 (2015), p.1-10

2015

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Determination of the botanical origin of honey by sensor fusion of impedance e-tongue and optical spectroscopy

Computers and electronics in agriculture, 2013-06, Vol.94, p.1-11

2013

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Regioselectivity in Hetero Diels–Alder Reactions

Journal of chemical education, 2019-01, Vol.96 (1), p.148-152

2019

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Photosensitizers for photodynamic therapy: One-pot heterogeneous catalytic transfer reduction of porphyrins

Journal of pharmacy & bioallied science, 2011-04, Vol.3 (2), p.294-297

2011

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[4+2] Cycloadditions of 3-Tetrazolyl-1,2-diaza-1,3-butadienes: Synthesis of 3-Tetrazolyl-1,4,5,6-tetrahydropyridazines

European journal of organic chemistry, 2012-04, Vol.2012 (11), p.2152-2160

2012

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Mild liquid-phase Friedel-Crafts acylation of heteroaromatic compounds over zeolite Beta

Journal of molecular catalysis. A, Chemical, 2009-06, Vol.305 (1), p.100-103

2009

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Metal-assisted reactions, Part 31 [1]: Adsorption isotherms and selective catalytic transfer reduction of aldehydes and ketones

Journal of molecular catalysis. A, Chemical, 2006-03, Vol.246 (1), p.100-108

2006

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Heteroaromatic benzyl ethers as intermediates for palladium-catalysed transfer hydrogenolysis of benzyl alcohols

Journal of molecular catalysis. A, Chemical, 2004-06, Vol.215 (1), p.113-120

2004

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Metal-Assisted Reactions. Part XXX. Control of Rates of Heterogeneously Catalyzed Transfer Hydrogenolysis through Changes in Solvent Composition

Australian journal of chemistry, 2003, Vol.56 (5), p.423

2003

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ChemInform Abstract: [4 + 2] Cycloadditions of 3-Tetrazolyl-1,2-diaza-1,3-butadienes: Synthesis of 3-Tetrazolyl-1,4,5,6-tetrahydropyridazines

ChemInform, 2012-08, Vol.43 (35), p.no-no

2012

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Structural effects on sigmatropic shifts in heteroaromatic allyl ethersElectronic supplementary information (ESI) available: selected crystal data for compound 7. See http://www.rsc.org/suppdata/p1/b1/b102674g

Perkin 1 : an international journal of organic and bio-organic chemistry, 2002-04 (9), p.1213-1219

2002

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Metal-assisted reactions. Part 24. The importance of solvents in liquid-phase heterogeneous catalytic transfer reduction

Tetrahedron, 1992-09, Vol.48 (36), p.7735-7746

1992

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Composition and in vitro antioxidants activity of Chamaerops humilis L

2017 IEEE 5th Portuguese Meeting on Bioengineering (ENBENG), 2017, p.1-4

2017

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Preparation of 3-Chloro-1,2-Benzisothiazole 1,1-Dioxide (Pseudo-Saccharyl Chloride)

Journal of chemical research, 2002-06, Vol.2002 (6), p.299-300

2002

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Heteroaromatic ethers of phenols in nickel-catalysed ipso-replacement reactions with magnesium, zinc and tin organometallic compounds

Perkin 1 : an international journal of organic and bio-organic chemistry, 2000-01 (11), p.1735-1739

2000

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Transition metal catalysed ipso-replacement reactions of heteroaromatic phenolic ethers by zinc and tin organometallic compounds

Journal of the Chemical Society. Chemical communications, 1994 (17), p.1923-1924

1994

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Mechanisms in heterogeneous liquid-phase catalytic-transfer reduction : the importance of hydrogen-donor concentration

Journal of the Chemical Society. Chemical communications, 1991 (15), p.1041-1042

1991

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3-(4-Methoxyphenoxy)-1,2-benzisothiazole 1,1-Dioxide: its Relation to Mechanistic Behaviour in Catalytic Transfer Hydrogenolysis

Acta crystallographica. Section C, Crystal structure communications, 1996-05, Vol.52 (5), p.1293-1296

1996

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Metal-assisted reactions. Part 29. Structure and hydrogenolysis of C–N bonds in derivatives of aromatic amines. Bond length and electronegativity changes from X-ray crystallographic data

Perkin 2 : an international journal of physical organic chemistry, 2001 (8), p.1315-1324

2001

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Metal-assisted reactions. Part 20. Catalytic transfer hydrogenolysis of phenolic CO bonds

Tetrahedron letters, 1990, Vol.31 (40), p.5789-5790

1990

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Electronic Effects on C-O-C Ether Bonds in 3-Aryloxy Derivatives of Benzisothiazole 1,1-Dioxides: Rapid Ethanolysis of 3-(4-Nitrophenoxy)-1,2-benzisothiazole 1,1-Dioxide, (1), to give 3-Ethoxy-1,2-benzisothiazole 1,1-Dioxide, (2)

Acta crystallographica. Section C, Crystal structure communications, 1998-02, Vol.54 (2), p.251-253

1998

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5-Benzyloxy-1-phenyltetrazole: catalytic transfer hydrogenolysis of benzyl ethers

Acta crystallographica. Section C, Crystal structure communications, 1999-05, Vol.55 (5), p.778-781

1999

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Thermal Rearrangement of 3-Allyloxy-1,2-Benzisothiazole 1,1-Dioxides: An Unusual Inversion of Products of Sigmatropic [3,3]-Shift to Give the [1,3]-Isomers

Journal of chemical research, 1999-12, Vol.23 (12), p.704-705

1999

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3-(1-Naphthyloxy)-1,2-benzisothiazole 1,1-Dioxide: Electronic Effects of Conjugation

Acta crystallographica. Section C, Crystal structure communications, 1996-06, Vol.52 (6), p.1576-1579

1996

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Metal-assisted reactions. Part 27.1 3-Benzyloxy-1,2-benzisothiazole 1,1-dioxide: an unusual ether linkage that does not permit heterogeneous catalytic hydrogenolysis

Journal of the Chemical Society, Perkin Transactions 1, 1997 (17), p.2603-2606

1997

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Physicochemical Parameters and Bioactive Compounds of Strawberry Tree (Arbutus unedo L.) Honey

Determination of the botanical origin of honey by sensor fusion of impedance e-tongue and optical spectroscopy

Regioselectivity in Hetero Diels–Alder Reactions

Photosensitizers for photodynamic therapy: One-pot heterogeneous catalytic transfer reduction of porphyrins

[4+2] Cycloadditions of 3-Tetrazolyl-1,2-diaza-1,3-butadienes: Synthesis of 3-Tetrazolyl-1,4,5,6-tetrahydropyridazines

Mild liquid-phase Friedel-Crafts acylation of heteroaromatic compounds over zeolite Beta

Metal-assisted reactions, Part 31 [1]: Adsorption isotherms and selective catalytic transfer reduction of aldehydes and ketones

Heteroaromatic benzyl ethers as intermediates for palladium-catalysed transfer hydrogenolysis of benzyl alcohols

Metal-Assisted Reactions. Part XXX. Control of Rates of Heterogeneously Catalyzed Transfer Hydrogenolysis through Changes in Solvent Composition

ChemInform Abstract: [4 + 2] Cycloadditions of 3-Tetrazolyl-1,2-diaza-1,3-butadienes: Synthesis of 3-Tetrazolyl-1,4,5,6-tetrahydropyridazines

Structural effects on sigmatropic shifts in heteroaromatic allyl ethersElectronic supplementary information (ESI) available: selected crystal data for compound 7. See http://www.rsc.org/suppdata/p1/b1/b102674g

Metal-assisted reactions. Part 24. The importance of solvents in liquid-phase heterogeneous catalytic transfer reduction

Composition and in vitro antioxidants activity of Chamaerops humilis L

Preparation of 3-Chloro-1,2-Benzisothiazole 1,1-Dioxide (Pseudo-Saccharyl Chloride)

Heteroaromatic ethers of phenols in nickel-catalysed ipso-replacement reactions with magnesium, zinc and tin organometallic compounds

Transition metal catalysed ipso-replacement reactions of heteroaromatic phenolic ethers by zinc and tin organometallic compounds

Mechanisms in heterogeneous liquid-phase catalytic-transfer reduction : the importance of hydrogen-donor concentration

3-(4-Methoxyphenoxy)-1,2-benzisothiazole 1,1-Dioxide: its Relation to Mechanistic Behaviour in Catalytic Transfer Hydrogenolysis

Metal-assisted reactions. Part 29. Structure and hydrogenolysis of C–N bonds in derivatives of aromatic amines. Bond length and electronegativity changes from X-ray crystallographic data

Metal-assisted reactions. Part 20. Catalytic transfer hydrogenolysis of phenolic CO bonds

Electronic Effects on C-O-C Ether Bonds in 3-Aryloxy Derivatives of Benzisothiazole 1,1-Dioxides: Rapid Ethanolysis of 3-(4-Nitrophenoxy)-1,2-benzisothiazole 1,1-Dioxide, (1), to give 3-Ethoxy-1,2-benzisothiazole 1,1-Dioxide, (2)

5-Benzyloxy-1-phenyltetrazole: catalytic transfer hydrogenolysis of benzyl ethers

Thermal Rearrangement of 3-Allyloxy-1,2-Benzisothiazole 1,1-Dioxides: An Unusual Inversion of Products of Sigmatropic [3,3]-Shift to Give the [1,3]-Isomers

3-(1-Naphthyloxy)-1,2-benzisothiazole 1,1-Dioxide: Electronic Effects of Conjugation

Metal-assisted reactions. Part 27.1 3-Benzyloxy-1,2-benzisothiazole 1,1-dioxide: an unusual ether linkage that does not permit heterogeneous catalytic hydrogenolysis

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