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A Sugar-Based Gelator for Marine Oil-Spill Recovery

Angewandte Chemie (International ed.), 2016-06, Vol.55 (27), p.7782-7785

International ed. in English, 2016

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How Far Are We in Combating Marine Oil Spills by Using Phase‐Selective Organogelators?

ChemSusChem, 2020-10, Vol.13 (20), p.5343-5360

2020

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Quantification of Noncovalent Interactions in Azide–Pnictogen, –Chalcogen, and –Halogen Contacts

Chemistry : a European journal, 2021-03, Vol.27 (14), p.4627-4639

2021

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Structure-based design of UDP-GlcNAc analogs as candidate GnT-V inhibitors

Biochimica et biophysica acta. General subjects, 2022-06, Vol.1866 (6), p.130118-130118, Article 130118

2022

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Model molecules to classify CH⋯O hydrogen-bonds

Chemical communications (Cambridge, England), 2018, Vol.54 (36), p.4629-4632

2018

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Regioselectivity among six secondary hydroxyl groups: selective acylation of the least reactive hydroxyl groups of inositol

Chemical communications (Cambridge, England), 2012-01, Vol.48 (18), p.2448-2450

2012

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Azide‐Functionalized Derivatives of the Virulence‐Associated Sugar Pseudaminic Acid: Chiral Pool Synthesis and Labeling of Bacteria

Chemistry : a European journal, 2021-07, Vol.27 (41), p.10595-10600

2021

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Advanced Chemical Methods for Stereoselective Sialylation and Their Applications in Sialoglycan Syntheses

Chemical record, 2021-11, Vol.21 (11), p.3194-3223

2021

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A versatile glycosylation strategy via Au(iii) catalyzed activation of thioglycoside donors

Chemical science (Cambridge), 2016-01, Vol.7 (7), p.4259-4263

2016

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Stereoselective Synthesis of Diglycosyl Diacylglycerols with Glycosyl Donors Bearing a β‑Stereodirecting 2,3-Naphthalenedimethyl Protecting Group

Journal of organic chemistry, 2020-12, Vol.85 (24), p.16166-16181

2020

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A Sugar-Based Gelator for Marine Oil-Spill Recovery

Angewandte Chemie, 2016-06, Vol.128 (27), p.7913-7916

2016

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Correction: Model molecules to classify CH O hydrogen-bonds

Chemical communications (Cambridge, England), 2018-01, Vol.54 (58), p.8136-8136

2018

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Triazolophostins: a library of novel and potent agonists of IP3 receptors

Organic & biomolecular chemistry, 2015-06, Vol.13 (24), p.6698-6710

2015

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Correction: A versatile glycosylation strategy via Au(iii) catalyzed activation of thioglycoside donors

Chemical science (Cambridge), 2016-09, Vol.7 (9), p.6282-6282

2016

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Strength from Weakness: Conformational Divergence between Solid and Solution States of Substituted Cyclitols Facilitated by CH···O Hydrogen Bonding

Journal of organic chemistry, 2014-06, Vol.79 (11), p.4892-4908

2014

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Synthesis of dimeric analogs of adenophostin A that potently evoke Ca2+ release through IP3 receptors

RSC advances, 2016-11, Vol.6 (89), p.86346-86351

2016

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Synthesis of dimeric analogs of adenophostin A that potently evoke Ca 2+ release through IP 3 receptors

RSC advances, 2016-11, Vol.6 (89), p.86346-86351

2016

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Strength from weakness: opportunistic CH···O hydrogen bonds differentially dictate the conformational fate in solid and solution states

Chemical communications (Cambridge, England), 2012-01, Vol.48 (5), p.717-719

2012

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Model molecules to classify CH O hydrogen-bondsElectronic supplementary information (ESI) available: Synthetic procedures, characterization, crystallographic, computational and spectral data for all new compounds. CCDC 1576754-1576760. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8cc01653d

2018-05

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A versatile glycosylation strategy via Au(iii) catalyzed activation of thioglycoside donorsElectronic supplementary information (ESI) available: Synthetic procedures, characterization and spectral data for all new compounds. See DOI: 10.1039/c6sc00633g

2016-06

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A versatile glycosylation strategy viaAu(iii) catalyzed activation of thioglycoside donors

Chemical science (Cambridge), 2016-06, Vol.7 (7), p.4259-4263

2016

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A versatile glycosylation strategy via Au(iii) catalyzed activation of thioglycoside donors† †Electronic supplementary information (ESI) available: Synthetic procedures, characterization and spectral data for all new compounds. See DOI: 10.1039/c6sc00633g

Chemical science (Cambridge), 2016-03, Vol.7 (7), p.4259-4263

2016

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Triazolophostins: a library of novel and potent agonists of IP3 receptorsElectronic supplementary information (ESI) available: Synthetic procedures and spectral data for all new compounds, crystal data for disaccharide 4 and details of the docking study. CCDC 1022279. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5ob00440c

2015-06

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Triazolophostins: a library of novel and potent agonists of IP3 receptors† †Electronic supplementary information (ESI) available: Synthetic procedures and spectral data for all new compounds, crystal data for disaccharide 4 and details of the docking study. CCDC 1022279. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5ob00440c Click here for additional data file. Click here for additional data file

Organic & biomolecular chemistry, 2015-04, Vol.13 (24), p.6698-6710

2015

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Triazolophostins: a library of novel and potent agonists of IP 3 receptors

Organic & biomolecular chemistry, 2015, Vol.13 (24), p.6698-6710

2015

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A Sugar-Based Gelator for Marine Oil-Spill Recovery

How Far Are We in Combating Marine Oil Spills by Using Phase‐Selective Organogelators?

Quantification of Noncovalent Interactions in Azide–Pnictogen, –Chalcogen, and –Halogen Contacts

Structure-based design of UDP-GlcNAc analogs as candidate GnT-V inhibitors

Model molecules to classify CH⋯O hydrogen-bonds

Regioselectivity among six secondary hydroxyl groups: selective acylation of the least reactive hydroxyl groups of inositol

Azide‐Functionalized Derivatives of the Virulence‐Associated Sugar Pseudaminic Acid: Chiral Pool Synthesis and Labeling of Bacteria

Advanced Chemical Methods for Stereoselective Sialylation and Their Applications in Sialoglycan Syntheses

A versatile glycosylation strategy via Au(iii) catalyzed activation of thioglycoside donors

Stereoselective Synthesis of Diglycosyl Diacylglycerols with Glycosyl Donors Bearing a β‑Stereodirecting 2,3-Naphthalenedimethyl Protecting Group

A Sugar-Based Gelator for Marine Oil-Spill Recovery

Correction: Model molecules to classify CH O hydrogen-bonds

Triazolophostins: a library of novel and potent agonists of IP3 receptors

Correction: A versatile glycosylation strategy via Au(iii) catalyzed activation of thioglycoside donors

Strength from Weakness: Conformational Divergence between Solid and Solution States of Substituted Cyclitols Facilitated by CH···O Hydrogen Bonding

Synthesis of dimeric analogs of adenophostin A that potently evoke Ca2+ release through IP3 receptors

Synthesis of dimeric analogs of adenophostin A that potently evoke Ca 2+ release through IP 3 receptors

Strength from weakness: opportunistic CH···O hydrogen bonds differentially dictate the conformational fate in solid and solution states

A versatile glycosylation strategy via Au(iii) catalyzed activation of thioglycoside donorsElectronic supplementary information (ESI) available: Synthetic procedures, characterization and spectral data for all new compounds. See DOI: 10.1039/c6sc00633g

A versatile glycosylation strategy viaAu(iii) catalyzed activation of thioglycoside donors

A versatile glycosylation strategy via Au(iii) catalyzed activation of thioglycoside donors† †Electronic supplementary information (ESI) available: Synthetic procedures, characterization and spectral data for all new compounds. See DOI: 10.1039/c6sc00633g

Triazolophostins: a library of novel and potent agonists of IP 3 receptors

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