The chemical synthesis of tetrodoxin: an ongoing quest (Q34231491)

31 July 2017

1 reference

17 September 2019

The chemical synthesis of tetrodoxin: an ongoing quest (English)

1 reference

31 July 2017

heterocyclic compound

1 reference

17 September 2019

Jaclyn Chau

1

1 reference

PubMed ID

22073009

31 July 2017

Marco A Ciufolini

series ordinal

2

1 reference

31 July 2017

20 October 2011

2 references

31 July 2017

17 September 2019

2 references

31 July 2017

17 September 2019

9

1 reference

31 July 2017

10

1 reference

31 July 2017

2046-2074

1 reference

Creative Commons Attribution 3.0 Unported

31 July 2017

1 reference

C-H functionalization logic in total synthesis

17 September 2019

0 references

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3210618

Tetrodotoxin for Moderate to Severe Cancer Pain: A Randomized, Double Blind, Parallel Design Multicenter Study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3210618

An efficient total synthesis of optically active tetrodotoxin

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3210618

A stereoselective synthesis of (-)-tetrodotoxin

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3210618

First asymmetric total synthesis of tetrodotoxin

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3210618

Asymmetric total synthesis of 11-deoxytetrodotoxin, a naturally occurring congener

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3210618

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3210618

Tetrodotoxin. VII. On the Structures of Tetrodotoxin and its Derivatives

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3210618

Synthetic approach towards tetrodotoxin. II. A stereospecific synthesis of a compound having the same six chiral centers on the cyclohexane ring as those of tetrodotoxin

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3210618

Synthetic intermediates potentially useful for the synthesis of tetrodotoxin and derivatives. II. Reaction of diazomethane with some shikimic acid derivatives

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3210618

Synthetic studies on tetrodotoxin and related compounds. IV. Stereospecific total syntheses of DL-tetrodotoxin

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3210618

Synthetic studies on tetrodotoxin and related compounds. 3. A stereospecific synthesis of an equivalent of acetylated tetrodamine

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3210618

Syntheses of tetrodotoxin.

6 July 2018

1 reference

The structure of tetrodotoxin

21 January 2018

1 reference

Reflections on the total synthesis of natural products: Art, craft, logic, and the chiron approach

21 January 2018

1 reference

An efficient total synthesis of optically active tetrodotoxin from levoglucosenone.

21 January 2018

1 reference

Stereocontrolled synthesis of 8,11-dideoxytetrodotoxin, unnatural analogue of puffer fish toxin.

21 January 2018

1 reference

Stereocontrolled synthesis of 8,11-dideoxytetrodotoxin, an unnatural analogue of puffer fish toxin

21 January 2018

1 reference

Novel and stereocontrolled synthesis of (+/-)-tetrodotoxin from myo-inositol

21 January 2018

1 reference

Stereoselective and efficient total synthesis of optically active tetrodotoxin from D-glucose

21 January 2018

1 reference

Synthesis of (-)-tetrodotoxin: preparation of an advanced cyclohexenone intermediate

21 January 2018

1 reference

5-exo Radical cyclization onto 3-alkoxyketimino-1, 6-anhydromannopyranoses. Efficient preparation of synthetic intermediates for (-)-tetrodotoxin.

21 January 2018

1 reference

Tandem phenolic oxidative amidation-intramolecular Diels-Alder reaction: an approach to the himandrine core

21 January 2018

1 reference

Total synthesis of tricyclic azaspirane derivatives of tyrosine: FR901483 and TAN1251C.

21 January 2018

1 reference

Approach to tetrodotoxin via the oxidative amidation of a phenol.

21 January 2018

1 reference

Synthetic approach towards tetrodotoxin. I. Diels-Alder reaction of α-oximinoethylbenzoquinones with butadiene

21 January 2018

1 reference

12 December 2020

Stereocontrolled Synthesis of (-)-5,11-Dideoxytetrodotoxin

1 reference

12 December 2020

Total synthesis of FR901483

1 reference

12 December 2020

Oxidation of oximes to nitrile oxides with hypervalent iodine reagents

1 reference

12 December 2020

Fully stereocontrolled total syntheses of (-)-cylindricine C and (-)-2-epicylindricine C: a departure in sulfonamide chemistry

1 reference

12 December 2020

Improved procedure for the bimolecular oxidative amidation of phenols

1 reference

12 December 2020

Nitrogenous educts through oxidative amidation of phenols: the bimolecular reaction

1 reference

12 December 2020

Oxidation of α-oxo-oximes to nitrile oxides with hypervalent iodine reagents

1 reference

12 December 2020

Oxidative spirocyclization of phenolic sulfonamides: scope and applications

1 reference

12 December 2020

New oxidative transformations of phenolic and indolic oxazolines: an avenue to useful azaspirocyclic building blocks

1 reference

12 December 2020

Intra- and intermolecular 1,3-dipolar cycloaddition of sugar ketonitrones with mono-, di-, and trisubstituted dipolarophiles

1 reference

12 December 2020

Armed/Disarmed Effects and Adamantyl Expansion of Some Caged Tricyclic Acetals en Route to Tetrodotoxin(1)(,)(2)

1 reference

12 December 2020

Identifiers

DOI

10.3390/MD9102046

1 reference

31 July 2017

1 reference

31 July 2017

1 reference

PubMed ID

22073009