(Q26744255)

5

object named as

Kazuhiko Otoguro

0 references

author name string

Yoshihiko Noguchi

1

0 references

Tomoyasu Hirose

2

0 references

Aki Ishiyama

3

0 references

Masato Iwatsuki

4

0 references

Toshiaki Sunazuka

Journal of Natural Medicines

6

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language of work or name

English

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publication date

July 2016

0 references

1 July 2016

4 references

22 June 2019

17 September 2019

7 November 2019

18 July 2021

1 reference

Creative Commons Attribution 4.0 International

volume

70

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issue

3

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page(s)

302-17

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copyright license

4 references

22 June 2019

17 September 2019

7 November 2019

Spiroindolones, a potent compound class for the treatment of malaria

18 July 2021

0 references

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Artemisinin-based combination therapies: a vital tool in efforts to eliminate malaria

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Artemisinin Resistance in Plasmodium falciparum Malaria

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Evidence of Artemisinin-Resistant Malaria in Western Cambodia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Qinghaosu (Artemisinin): The Price of Success

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Malaria: progress, perils, and prospects for eradication

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Benzylic Substitution of Gramines with Boronic Acids and Rhodium or Iridium Catalysts†

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Angustilobine and andranginine type indole alkaloids and an uleine-secovallesamine bisindole alkaloid from Alstonia angustiloba.

25 May 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Synthesis of conolidine, a potent non-opioid analgesic for tonic and persistent pain.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Borrelidin, a potent antimalarial: stage-specific inhibition profile of synchronized cultures of Plasmodium falciparum

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Total synthesis of (+)-condylocarpine, (+)-isocondylocarpine, and (+)-tubotaiwine

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

In vitro and in vivo antimalarial activity of puberulic acid and its new analogs, viticolins A–C, produced by Penicillium sp. FKI-4410

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Direct organocatalytic coupling of carboxylated piperazine-2,5-diones with indoles through conjugate addition of carbon nucleophiles to indolenine intermediates

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

DNA adducts of aristolochic acid II: total synthesis and site-specific mutagenesis studies in mammalian cells

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

New medicines to improve control and contribute to the eradication of malaria

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Enhancement of chemically-induced HL-60 cell differentiation by 3,3'-diindolylmethane derivatives

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

The global portfolio of new antimalarial medicines under development.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

A new family of tunable indolylphosphine ligands by one-pot assembly and their applications in Suzuki-Miyaura coupling of aryl chlorides

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Coupling of activated esters to gramines in the presence of ethyl propiolate under mild conditions

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Concise, asymmetric, stereocontrolled total synthesis of stephacidins A, B and notoamide B

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Antimalarial drugs and pregnancy: safety, pharmacokinetics, and pharmacovigilance.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Biologically active ibogan and vallesamine derivatives from Tabernaemontana divaricata

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Novel bis(1H-indol-2-yl)methanones as potent inhibitors of FLT3 and platelet-derived growth factor receptor tyrosine kinase

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Medical need, scientific opportunity and the drive for antimalarial drugs

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Potent antimalarial activities of polyether antibiotic, X-206.

28 September 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

28 September 2017

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

7 January 2021

Isolation of opioid-active compounds from Tabernaemontana pachysiphon leaves

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Structure determination and total synthesis of (+)-16-hydroxy-16,22-dihydroapparicine

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Indole alkaloids from Tabernaemontana elegans.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

Indole alkaloids from the leaves of Philippine Alstonia scholaris

31 May 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

The first total synthesis of (+/-)-apparicine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

Total synthesis of the bridged indole alkaloid apparicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

Enantiospecific Synthesis of (R)-4-Amino-5-oxo-1,3,4,5-tetrahydrobenz[cd]indole, an Advanced Intermediate Containing the Tricyclic Core of the Ergots

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

Synthesis of N-protected staurosporinones

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

Trapping of the putative cationic intermediate in the Morin rearrangement with carbon nucleophiles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

(1-nosyl-5-nitroindol-3-yl)methyl ester: a novel protective group for carboxylic acids.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

Über neue organische Phosphorverbindungen III. Phosphinmethylenderivate und Phosphinimine

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

Around and beyond Cram's Rule.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

Allylic 1,3-strain as a controlling factor in stereoselective transformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

Total Synthesis of (-)-Furaquinocin C

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

1,2-dioxines as masked cis gamma-hydroxy enones and their versatility in the synthesis of highly substituted gamma-lactones.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

Total synthesis of (+)-neomarinone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

21 January 2018

Rules for ring closure

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

A protecting group free synthesis of (+/-)-neostenine via the [5 + 2] photocycloaddition of maleimides

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

Synthesis of thiazino[6,5-b]indole derivatives, analogues of the phytoalexin cyclobrassinin. A new method for preparation of 3-aminomethylindole

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

Malaria research in the post-genomic era

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935745

In vitro and in vivo antimalarial activities of the monoglycoside polyether antibiotic, K-41 against drug resistant strains of Plasmodia

28 November 2018

1 reference

12 December 2020

Convergent approach to the tetracyclic core of the apparicine class of indole alkaloids via a key intermolecular nitrosoalkene conjugate addition

1 reference

12 December 2020

A Concise Total Synthesis of the Notoamides C and D

1 reference

12 December 2020

Spiroquinazoline Support Studies: New Cascade Reactions Based on the Morin Rearrangement

1 reference

12 December 2020

The use of sulfur ylides in the synthesis of substituted indoles

1 reference

12 December 2020

Alkaloid studies. L. The alkaloids of twelve Aspidosperma species

1 reference

12 December 2020

Epchrosine - a new indole alkaloid isolated from plant cell cultures of Ochrosia elliptica Labill

1 reference

12 December 2020

Inhibition of FLT3 and PDGFR tyrosine kinase activity by bis(benzo[b]furan-2-yl)methanones

1 reference

12 December 2020

Phosphine-mediated coupling of gramines with aldehydes: a remarkably simple synthesis of 3-vinylindoles

1 reference

12 December 2020

Alkaloid studies. 48. The structure of apparicine, a novel Aspidosperma alkaloid

1 reference

12 December 2020

Antimicrobial, antiamoebic and antiviral screening of some Tabernaemontana species

1 reference

12 December 2020

A synthesis of the diazonamide heteroaromatic biaryl macrocycle/hemiaminal core

1 reference

12 December 2020

Synthesis and confirmation of structure for the gibberellin GA131 (18-hydroxy-GA4)

1 reference

12 December 2020

Alkaloids from leaves and bark ofAlstonia scholaris in the Philippines

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

7 January 2021

Biomimetic oxidative transformations of pericine: partial synthesis of apparicine and valparicine, a new pentacyclic indole alkaloid from Kopsia

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

7 January 2021

Study of the catalytic properties of tris (3,6-dioxaheptyl) amine (tda-1) in heteroaromatic nucleophilic substitution of chloropyridines and their n-oxides

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

7 January 2021

16(S)-Hydroxy-16,22-dihydroapparicine, a New Alkaloid from the Leaves of Tabernaemontana dichotoma

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

7 January 2021

Antimicrobially Active Alkaloids from Tabernaemontana chippii

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

7 January 2021

Some New Vallesamine-Type Alkaloids

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

7 January 2021

One-Pot Desulfonylative Alkylation of N-Sulfonyl Azacycles Using Alkoxides Generated by Phase-Transfer Catalysis

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

7 January 2021

Indole Alkaloids fromTabernaemontana elegans1

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

7 January 2021

The Isolation and Structure of Ervaticine, a New Indole Alkaloid from Ervatamia coronaria

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

7 January 2021

Isolation of 19,20-Z-Vallesamine and 19,20-E-Vallesamine from Alstonia scholaris

1 reference

https://api.crossref.org/works/10.1007%2FS11418-016-1012-2

7 January 2021

10.1007/S11418-016-1012-2

Identifiers

DOI

1 reference

Dimensions Publication ID

1036596225

0 references

1 reference

1 reference

PubMed publication ID

27324906

1 reference