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Facile Synthesis of Enantiomerically Pure 2‐ and 2,3‐Disubstituted Furans Catalysed by Mixed Lewis Acids: An Easy Route to 3‐Iodofurans and 3‐(Hydroxymethyl)furans

Chemistry : a European journal, 2009-06, Vol.15 (24), p.6041-6049

2009

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Chiral Pyridin-3-ones and Pyridines: Syntheses of Enantiopure 2,4-Disubstituted 6-Hydroxy-1,6-Dihydro-2H-Pyridin-3-ones, 2,3-Disubstituted 4-Iodopyridines, and Enantiopure 2,3-Disubstituted 4-Pyridinemethanols

Journal of organic chemistry, 2011-11, Vol.76 (21), p.8930-8943

2011

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A Chiron Approach to Aminocytitols by Petasis-Borono-Mannich Reaction: Formal Synthesis of (+)-Conduramine E and (−)-Conduramine E

Journal of organic chemistry, 2012-09, Vol.77 (17), p.7627-7632

2012

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The evolution of comprehensive strategies for furanoid glycal synthesis and their applications

RSC advances, 2017-01, Vol.7 (42), p.25897-25963

2017

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Glycal approach to the synthesis of macrolide (−)-A26771B

RSC advances, 2015-01, Vol.5 (37), p.29114-29120

2015

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Glycal-Derived δ‑Hydroxy α,β-Unsaturated Aldehydes (Perlin Aldehydes): Versatile Building Blocks in Organic Synthesis

Chemical reviews, 2013-05, Vol.113 (5), p.3605-3631

2013

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‘Chiron’ approach to stereoselective synthesis of sphinganine and unnatural safingol, an antineoplastic and antipsoriatic agent

RSC advances, 2016-01, Vol.6 (18), p.14505-14511

2016

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Stereoselective total syntheses of (+)- exo- and (−)- exo-brevicomins, (+)- endo- and (−)- endo-brevicomins, (+)- and (−)-cardiobutanolides, (+)-goniofufurone

Tetrahedron, 2011-06, Vol.67 (22), p.4036-4047

2011

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‘Chiron’ approach to the total synthesis of macrolide (+)-Aspicilin

RSC advances, 2014-01, Vol.4 (9), p.4253-4259

2014

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An efficient total synthesis of the anticancer agent (+)-spisulosine (ES-285) from Garner’s aldehyde

Tetrahedron letters, 2010-08, Vol.51 (31), p.4140-4142

2010

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First Total Synthesis of (+)-Varitriol

Journal of organic chemistry, 2008-10, Vol.73 (19), p.7526-7531

2008

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Arsenate (AsV) stress response in maize (Zea mays L.)

Environmental and experimental botany, 2016-10, Vol.130, p.53-67

2016

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Design, synthesis and biological evaluation of bicyclic iminosugar hybrids: conformational constraint as an effective tool for tailoring the selectivity of α-glucosidase inhibitors

Organic & biomolecular chemistry, 2014-09, Vol.12 (35), p.6855-6868

2014

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Aglycone mimics for tuning of glycosidase inhibition: design, synthesis and biological evaluation of bicyclic pyrrolidotriazole iminosugars

RSC advances, 2016-01, Vol.6 (16), p.13014-13026

2016

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CP-MLR directed QSAR studies on the antimycobacterial activity of functionalized alkenols—topological descriptors in modeling the activity

Bioorganic & medicinal chemistry, 2005-01, Vol.13 (2), p.343-351

2005

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Diastereoselective one-pot Wittig olefination-Michael addition and olefin cross metathesis strategy for total synthesis of cytotoxic natural product (+)-varitriol and its higher analogues

Organic & biomolecular chemistry, 2011-11, Vol.9 (21), p.7372-7383

2011

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Syntheses of (−)-gabosine A, (+)-4- epi-gabosine A, (−)-gabosine E, and (+)-4- epi-gabosine E

Tetrahedron, 2011-06, Vol.67 (25), p.4539-4546

2011

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A chiron approach to the total synthesis of cytotoxic (+)-muricatacin and (+)-5- epi-muricatacin from d-ribose

Carbohydrate research, 2010-01, Vol.345 (1), p.41-44

2010

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β-aminobutyric acid mediated drought stress alleviation in maize (Zea mays L.)

Environmental science and pollution research international, 2016-02, Vol.23 (3), p.2437-2453

2016

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Substrate and stereocontrolled iodocycloetherification of highly functionalized enantiomerically pure allylic alcohols: application to synthesis of cytotoxic 2-epi jaspine B and its biological evaluation

Organic & biomolecular chemistry, 2015-08, Vol.13 (30), p.8241-8250

2015

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Synthesis of 2,3,6-trideoxy sugar triazole hybrids as potential new broad spectrum antimicrobial agents

European journal of medicinal chemistry, 2014-08, Vol.83, p.474-489

2014

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A convergent total synthesis of a new antiepileptic ceramide and its triacetyl derivative using olefin cross metathesis

Tetrahedron, 2010-09, Vol.66 (38), p.7504-7509

2010

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A Substrate‐Directed Diastereoselective Synthesis of Vicinal Diamines Using an A3‐Coupling Strategy: An Application to the Total Synthesis of (+)‐ and (−)‐Epiquinamides

Asian journal of organic chemistry, 2017-05, Vol.6 (5), p.503-506

2017

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Correction: Aglycone mimics for tuning of glycosidase inhibition: design, synthesis and biological evaluation of bicyclic pyrrolidotriazole iminosugars

RSC advances, 2016-03, Vol.6 (29), p.24683-24683

2016

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Conjugation-Driven Cascade Approach to Enantiopure Pyrano-Fused 1,5-Benzodiazepines by Tandem Condensation/[3,3]-Sigmatropic Rearrangement/Aza-Michael Addition-Elimination

European journal of organic chemistry, 2013-04, Vol.2013 (11), p.2194-2200

2013

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Facile Synthesis of Enantiomerically Pure 2‐ and 2,3‐Disubstituted Furans Catalysed by Mixed Lewis Acids: An Easy Route to 3‐Iodofurans and 3‐(Hydroxymethyl)furans

Chiral Pyridin-3-ones and Pyridines: Syntheses of Enantiopure 2,4-Disubstituted 6-Hydroxy-1,6-Dihydro-2H-Pyridin-3-ones, 2,3-Disubstituted 4-Iodopyridines, and Enantiopure 2,3-Disubstituted 4-Pyridinemethanols

A Chiron Approach to Aminocytitols by Petasis-Borono-Mannich Reaction: Formal Synthesis of (+)-Conduramine E and (−)-Conduramine E

The evolution of comprehensive strategies for furanoid glycal synthesis and their applications

Glycal approach to the synthesis of macrolide (−)-A26771B

Glycal-Derived δ‑Hydroxy α,β-Unsaturated Aldehydes (Perlin Aldehydes): Versatile Building Blocks in Organic Synthesis

‘Chiron’ approach to stereoselective synthesis of sphinganine and unnatural safingol, an antineoplastic and antipsoriatic agent

Stereoselective total syntheses of (+)- exo- and (−)- exo-brevicomins, (+)- endo- and (−)- endo-brevicomins, (+)- and (−)-cardiobutanolides, (+)-goniofufurone

‘Chiron’ approach to the total synthesis of macrolide (+)-Aspicilin

An efficient total synthesis of the anticancer agent (+)-spisulosine (ES-285) from Garner’s aldehyde

First Total Synthesis of (+)-Varitriol

Arsenate (AsV) stress response in maize (Zea mays L.)

Design, synthesis and biological evaluation of bicyclic iminosugar hybrids: conformational constraint as an effective tool for tailoring the selectivity of α-glucosidase inhibitors

Aglycone mimics for tuning of glycosidase inhibition: design, synthesis and biological evaluation of bicyclic pyrrolidotriazole iminosugars

CP-MLR directed QSAR studies on the antimycobacterial activity of functionalized alkenols—topological descriptors in modeling the activity

Diastereoselective one-pot Wittig olefination-Michael addition and olefin cross metathesis strategy for total synthesis of cytotoxic natural product (+)-varitriol and its higher analogues

Syntheses of (−)-gabosine A, (+)-4- epi-gabosine A, (−)-gabosine E, and (+)-4- epi-gabosine E

A chiron approach to the total synthesis of cytotoxic (+)-muricatacin and (+)-5- epi-muricatacin from d-ribose

β-aminobutyric acid mediated drought stress alleviation in maize (Zea mays L.)

Substrate and stereocontrolled iodocycloetherification of highly functionalized enantiomerically pure allylic alcohols: application to synthesis of cytotoxic 2-epi jaspine B and its biological evaluation

Synthesis of 2,3,6-trideoxy sugar triazole hybrids as potential new broad spectrum antimicrobial agents

A convergent total synthesis of a new antiepileptic ceramide and its triacetyl derivative using olefin cross metathesis

A Substrate‐Directed Diastereoselective Synthesis of Vicinal Diamines Using an A3‐Coupling Strategy: An Application to the Total Synthesis of (+)‐ and (−)‐Epiquinamides

Correction: Aglycone mimics for tuning of glycosidase inhibition: design, synthesis and biological evaluation of bicyclic pyrrolidotriazole iminosugars

Conjugation-Driven Cascade Approach to Enantiopure Pyrano-Fused 1,5-Benzodiazepines by Tandem Condensation/[3,3]-Sigmatropic Rearrangement/Aza-Michael Addition-Elimination

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