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Laccase-catalyzed coupling of catharanthine and vindoline: an efficient approach to the bisindole alkaloid anhydrovinblastine

Tetrahedron, 2009-01, Vol.65 (1), p.312-317

2009

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Synthesis and biological evaluation of new camptothecin derivatives obtained by modification of position 20

Bioorganic & medicinal chemistry, 2010-12, Vol.18 (24), p.8660-8668

2010

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Concise asymmetric synthesis of (−)-halosaline and (2 R,9a R)-(+)-2-hydroxy-quinolizidine by ruthenium-catalyzed ring-rearrangement metathesis

Tetrahedron, 2004-07, Vol.60 (31), p.6437-6442

2004

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Short enantioselective synthesis of sedridines, ethylnorlobelols and coniine via reagent-based differentiation

Tetrahedron: asymmetry, 2005-07, Vol.16 (13), p.2225-2229

2005

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Enzyme assisted enantioselective synthesis of the alkaloid (+)-aloperine

Tetrahedron: asymmetry, 2004-09, Vol.15 (18), p.2921-2925

2004

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Synthesis and biological evaluation of pyrroloiminoquinone derivatives

Bioorganic & medicinal chemistry, 2008-03, Vol.16 (5), p.2431-2438

2008

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New solution free and polymer anchored chiral bispidine-based amino alcohols. Synthesis and screening for the enantioselective addition of diethylzinc to benzaldehyde

Tetrahedron: asymmetry, 2003-08, Vol.14 (16), p.2453-2458

2003

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Dual targeted 2-Benzylideneindanone pendant hydroxamic acid group exhibits selective HDAC6 inhibition along with tubulin stabilization effect

Bioorganic & medicinal chemistry, 2023-05, Vol.86, p.117300-117300, Article 117300

2023

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Synthetic approach to imidazo[1,2- a]pyridine derivatives by the intramolecular nitrone cycloaddition methodology

Tetrahedron, 2002-05, Vol.58 (22), p.4445-4450

2002

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Synthesis and biological evaluation of imidazolo[2,1-b]benzothiazole derivatives, as potential p53 inhibitors

Bioorganic & medicinal chemistry, 2011-03, Vol.19 (5), p.1649-1657

2011

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‘Click’ synthesis of a triazole-based inhibitor of Met functions in cancer cells

Bioorganic & medicinal chemistry letters, 2012-07, Vol.22 (14), p.4693-4696

2012

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Inhibitors of tubulin polymerization: Synthesis and biological evaluation of hybrids of vindoline, anhydrovinblastine and vinorelbine with thiocolchicine, podophyllotoxin and baccatin III

Bioorganic & medicinal chemistry, 2008-06, Vol.16 (11), p.6269-6285

2008

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Tubulin-guided dynamic combinatorial library of thiocolchicine–podophyllotoxin conjugates

Tetrahedron, 2011-09, Vol.67 (38), p.7354-7357

2011

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Quinazolinecarboline alkaloid evodiamine as scaffold for targeting topoisomerase I and sirtuins

Bioorganic & medicinal chemistry, 2013-11, Vol.21 (22), p.6920-6928

2013

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Synthesis and biological evaluation of novel tamoxifen analogues

Bioorganic & medicinal chemistry, 2013-07, Vol.21 (14), p.4120-4131

2013

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Histone deacetylase and microtubules as targets for the synthesis of releasable conjugate compounds

Bioorganic & medicinal chemistry letters, 2009-11, Vol.19 (22), p.6358-6363

2009

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Enantiopure 2-piperidylacetaldehyde as a useful building block in the diversity-oriented synthesis of polycyclic piperidine derivatives

Tetrahedron: asymmetry, 2011-02, Vol.22 (3), p.264-269

2011

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Biomimetic construction of the tetracyclic ring system of ngouniensine

Tetrahedron, 1999-12, Vol.55 (52), p.14995-15000

1999

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Synthesis and biological evaluation of epothilone A dimeric compounds

Bioorganic & medicinal chemistry, 2009-11, Vol.17 (21), p.7435-7440

2009

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An enantioselective synthesis of the Strychnos alkaloid (−)-tubifoline

Tetrahedron: asymmetry, 1996-10, Vol.7 (10), p.2775-2778

1996

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Chiral diamines for asymmetric synthesis: an efficient RCM construction of the ligand core of (−)- and (+)-sparteine

Tetrahedron letters, 2005-10, Vol.46 (42), p.7121-7123

2005

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Enantiopure N-Boc piperidine-2-ethanol for the synthesis of (+)- and (−)-dumetorine, and (+)- and (−)-epidihydropinidine

Tetrahedron: asymmetry, 2009-02, Vol.20 (2), p.192-197

2009

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Stereocontrolled synthesis of enantiopure cis- and trans-3,4,4a,5,8,8a-hexahydro-1H-quinolin-2-ones

Tetrahedron: asymmetry, 2008-10, Vol.19 (20), p.2406-2410

2008

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Studies on oxidation of ergot alkaloids: oxidation and desaturation of dihydrolysergol—stereochemical requirements

Tetrahedron, 2007-10, Vol.63 (42), p.10466-10478

2007

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Synthesis of enantiopure diamine ligands related to sparteine, via scandium triflate-catalyzed imino Diels–Alder reactions

Tetrahedron letters, 2002-09, Vol.43 (40), p.7155-7158

2002

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Laccase-catalyzed coupling of catharanthine and vindoline: an efficient approach to the bisindole alkaloid anhydrovinblastine

Synthesis and biological evaluation of new camptothecin derivatives obtained by modification of position 20

Concise asymmetric synthesis of (−)-halosaline and (2 R,9a R)-(+)-2-hydroxy-quinolizidine by ruthenium-catalyzed ring-rearrangement metathesis

Short enantioselective synthesis of sedridines, ethylnorlobelols and coniine via reagent-based differentiation

Enzyme assisted enantioselective synthesis of the alkaloid (+)-aloperine

Synthesis and biological evaluation of pyrroloiminoquinone derivatives

New solution free and polymer anchored chiral bispidine-based amino alcohols. Synthesis and screening for the enantioselective addition of diethylzinc to benzaldehyde

Dual targeted 2-Benzylideneindanone pendant hydroxamic acid group exhibits selective HDAC6 inhibition along with tubulin stabilization effect

Synthetic approach to imidazo[1,2- a]pyridine derivatives by the intramolecular nitrone cycloaddition methodology

Synthesis and biological evaluation of imidazolo[2,1-b]benzothiazole derivatives, as potential p53 inhibitors

‘Click’ synthesis of a triazole-based inhibitor of Met functions in cancer cells

Inhibitors of tubulin polymerization: Synthesis and biological evaluation of hybrids of vindoline, anhydrovinblastine and vinorelbine with thiocolchicine, podophyllotoxin and baccatin III

Tubulin-guided dynamic combinatorial library of thiocolchicine–podophyllotoxin conjugates

Quinazolinecarboline alkaloid evodiamine as scaffold for targeting topoisomerase I and sirtuins

Synthesis and biological evaluation of novel tamoxifen analogues

Histone deacetylase and microtubules as targets for the synthesis of releasable conjugate compounds

Enantiopure 2-piperidylacetaldehyde as a useful building block in the diversity-oriented synthesis of polycyclic piperidine derivatives

Biomimetic construction of the tetracyclic ring system of ngouniensine

Synthesis and biological evaluation of epothilone A dimeric compounds

An enantioselective synthesis of the Strychnos alkaloid (−)-tubifoline

Chiral diamines for asymmetric synthesis: an efficient RCM construction of the ligand core of (−)- and (+)-sparteine

Enantiopure N-Boc piperidine-2-ethanol for the synthesis of (+)- and (−)-dumetorine, and (+)- and (−)-epidihydropinidine

Stereocontrolled synthesis of enantiopure cis- and trans-3,4,4a,5,8,8a-hexahydro-1H-quinolin-2-ones

Studies on oxidation of ergot alkaloids: oxidation and desaturation of dihydrolysergol—stereochemical requirements

Synthesis of enantiopure diamine ligands related to sparteine, via scandium triflate-catalyzed imino Diels–Alder reactions

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