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Langmuir-Blodgett monolayers holding a wound healing active compound and its effect in cell culture. A model for the study of surface mediated drug delivery systems

Heliyon, 2021-03, Vol.7 (3), p.e06436-e06436, Article e06436

2021

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Synthetic approaches to carnegine, a simple tetrahydroisoquinoline alkaloid

Tetrahedron, 2004-11, Vol.60 (47), p.10575-10610

2004

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Recent developments in the total synthesis of natural products using the Ugi multicomponent reactions as the key strategy

Organic & biomolecular chemistry, 2024-01, Vol.22 (3), p.429-465

2024

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Furo[3,2-]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms

RSC advances, 2020-09, Vol.1 (55), p.33344-33377

2020

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Angular tricyclic benzofurans and related natural products of fungal origin. Isolation, biological activity and synthesis

Natural product reports, 2013-01, Vol.3 (7), p.941-969

2013

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Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid

RSC advances, 2020-05, Vol.1 (32), p.18978-192

2020

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Synthesis and evaluation of aromatic methoxime derivatives against five postharvest phytopathogenic fungi of fruits. Main structure–activity relationships

Food chemistry, 2020-08, Vol.321, p.126701-126701, Article 126701

2020

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A concise Friedländer/Buchwald-Hartwig approach to the total synthesis of quindoline, a bioactive natural indoloquinoline alkaloid, and toward the unnatural 10-methylquindoline

New journal of chemistry, 2019-07, Vol.43 (27), p.183-1813

2019

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Efficient Buchwald-Hartwig and nitrene-mediated five-membered ring closure approaches to the total synthesis of quindoline. Unexpected direct conversion of a nitro group into a phosphazene

RSC advances, 2023-05, Vol.13 (2), p.13715-13724

2023

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Neocryptolepine (Cryprotackieine), A Unique Bioactive Natural Product: Isolation, Synthesis, and Profile of Its Biological Activity

European journal of organic chemistry, 2014-12, Vol.2014 (36), p.7979-8003

2014

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Total syntheses of gerberinol I and the pterophyllins 2 and 4 using the Casnati-Skattebøl reaction under different conditions

Organic & biomolecular chemistry, 2017-08, Vol.15 (33), p.7040-7049

2017

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Synthesis and interaction of terminal unsaturated chemical probes with Mycobacterium tuberculosis CYP124A1

Bioorganic & medicinal chemistry, 2021-08, Vol.44, p.116304-116304, Article 116304

2021

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Efficient total synthesis of neocryptolepine and synthetic access to 6-methylquinindoline from a common intermediate

RSC advances, 2017, Vol.7 (45), p.28298-28307

2017

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Experimental and theoretical studies of the [3,3]-sigmatropic rearrangement of prenyl azides

RSC advances, 2017, Vol.7 (75), p.47527-47538

2017

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Relevant Developments in the Use of Three‐Component Reactions for the Total Synthesis of Natural Products. The last 15 Years

ChemistryOpen (Weinheim), 2024-05, Vol.13 (5), p.e202300306-n/a

2024

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A convenient and eco-friendly cerium(III) chloride-catalysed synthesis of methoxime derivatives of aromatic aldehydes and ketones

Royal Society open science, 2018-05, Vol.5 (5), p.180279-180279

2018

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Expedient Approach to 6-Bromo-2-isopropylidenecoumaranone, a Potential Intermediate for the Synthesis of TMC-120B, Pseudodeflectusin, and Their Congeners

Helvetica chimica acta, 2016-05, Vol.99 (5), p.398-404

2016

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Synthesis of the unique angular tricyclic chromone structure proposed for aspergillitine, and its relationship with alkaloid TMC-120B

Organic & biomolecular chemistry, 2012-05, Vol.10 (20), p.4124-4134

2012

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Synthesis of the Carbon Framework of the Stephaoxocanes Employing a Sequential RCM/Pomeranz-Fritsch Approach

European Journal of Organic Chemistry, 2007-11, Vol.2007 (31), p.5284-5293

2007

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Electrocyclization‐Mediated Approach to 2‐Methyltriclisine, an Unnatural Analog of the Azafluoranthene Alkaloid Triclisine

European Journal of Organic Chemistry, 2009-09, Vol.2009 (27), p.4637-4645

2009

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Activity of the pterophyllins 2 and 4 against postharvest fruit pathogenic fungi. Comparison with a synthetic analog and related intermediates

Fitoterapia, 2018-03, Vol.125, p.98-105

2018

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Synthesis of tricyclic analogs of stephaoxocanidine and their evaluation as acetylcholinesterase inhibitors

Bioorganic & medicinal chemistry letters, 2005-06, Vol.15 (11), p.2711-2715

2005

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Economical and Convenient Carbonyl Transposition Approach Toward a 2-Arylcycloheptanone Derivative

Synthetic communications, 2006-01, Vol.36 (3), p.299-310

2006

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An alternative and convenient synthesis of oct-7-enal, a naturally-occurring aldehyde isolated from the Japanese thistle Cirsium dipsacolepis

Journal of the Brazilian Chemical Society, 2008, Vol.19 (6), p.1125-1128

2008

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Langmuir-Blodgett monolayers holding a wound healing active compound and its effect in cell culture. A model for the study of surface mediated drug delivery systems

Synthetic approaches to carnegine, a simple tetrahydroisoquinoline alkaloid

Recent developments in the total synthesis of natural products using the Ugi multicomponent reactions as the key strategy

Furo[3,2-]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms

Angular tricyclic benzofurans and related natural products of fungal origin. Isolation, biological activity and synthesis

Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid

Synthesis and evaluation of aromatic methoxime derivatives against five postharvest phytopathogenic fungi of fruits. Main structure–activity relationships

A concise Friedländer/Buchwald-Hartwig approach to the total synthesis of quindoline, a bioactive natural indoloquinoline alkaloid, and toward the unnatural 10-methylquindoline

Efficient Buchwald-Hartwig and nitrene-mediated five-membered ring closure approaches to the total synthesis of quindoline. Unexpected direct conversion of a nitro group into a phosphazene

Neocryptolepine (Cryprotackieine), A Unique Bioactive Natural Product: Isolation, Synthesis, and Profile of Its Biological Activity

Total syntheses of gerberinol I and the pterophyllins 2 and 4 using the Casnati-Skattebøl reaction under different conditions

Synthesis and interaction of terminal unsaturated chemical probes with Mycobacterium tuberculosis CYP124A1

Efficient total synthesis of neocryptolepine and synthetic access to 6-methylquinindoline from a common intermediate

Experimental and theoretical studies of the [3,3]-sigmatropic rearrangement of prenyl azides

Relevant Developments in the Use of Three‐Component Reactions for the Total Synthesis of Natural Products. The last 15 Years

A convenient and eco-friendly cerium(III) chloride-catalysed synthesis of methoxime derivatives of aromatic aldehydes and ketones

Expedient Approach to 6-Bromo-2-isopropylidenecoumaranone, a Potential Intermediate for the Synthesis of TMC-120B, Pseudodeflectusin, and Their Congeners

Synthesis of the unique angular tricyclic chromone structure proposed for aspergillitine, and its relationship with alkaloid TMC-120B

Synthesis of the Carbon Framework of the Stephaoxocanes Employing a Sequential RCM/Pomeranz-Fritsch Approach

Electrocyclization‐Mediated Approach to 2‐Methyltriclisine, an Unnatural Analog of the Azafluoranthene Alkaloid Triclisine

Activity of the pterophyllins 2 and 4 against postharvest fruit pathogenic fungi. Comparison with a synthetic analog and related intermediates

Synthesis of tricyclic analogs of stephaoxocanidine and their evaluation as acetylcholinesterase inhibitors

Economical and Convenient Carbonyl Transposition Approach Toward a 2-Arylcycloheptanone Derivative

An alternative and convenient synthesis of oct-7-enal, a naturally-occurring aldehyde isolated from the Japanese thistle Cirsium dipsacolepis

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