(Q33958550)

30 July 2017

title

New synthetic technology for the construction of N-hydroxyindoles and synthesis of nocathiacin I model systems (English)

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30 July 2017

K C Nicolaou

1

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30 July 2017

Anthony A Estrada

2

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30 July 2017

Graeme C Freestone

3

1 reference

30 July 2017

Sang Hyup Lee

4

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30 July 2017

Xavier Alvarez-Mico

5

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30 July 2017

publication date

1 July 2007

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30 July 2017

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30 July 2017

volume

63

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30 July 2017

issue

27

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30 July 2017

page(s)

6088-6114

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Total synthesis of thiostrepton. Retrosynthetic analysis and construction of key building blocks

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896327

5 July 2018

Thiopeptide antibiotics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896327

MJ347-81F4 A & B, novel antibiotics from Amycolatopsis sp.: taxonomic characteristics, fermentation, and antimicrobial activity.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896327

Efficient synthesis of N-methoxyindoles via alkylative cycloaddition of nitrosoarenes with alkynes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896327

A general synthesis of N-hydroxyindoles

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896327

Nocathiacins, new thiazolyl peptide antibiotics from Nocardia sp. II. Isolation, characterization, and structure determination

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896327

Nocathiacins, new thiazolyl peptide antibiotics from Nocardia sp. I. Taxonomy, fermentation and biological activities.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896327

Conformation and absolute configuration of nocathiacin I determined by NMR spectroscopy and chiral capillary electrophoresis

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896327

Synthesis of tricyclic indole-2-carboxylic [correction of caboxylic] acids as potent NMDA-glycine antagonists

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896327

Identification of a Novel Michael Acceptor Group for the Reversible Addition of Oxygen- and Sulfur-Based Nucleophiles. Synthesis and Reactivity of the 3-Alkylidene-3H-indole 1-Oxide Function of Avrainvillamide

29 October 2018

1 reference

12 December 2020

Synthesis of highly substituted N-hydroxyindoles through 1,5-addition of carbon nucleophiles to in situ generated unsaturated nitrones

1 reference

12 December 2020

A mild and selective method for the hydrolysis of esters with trimethyltin hydroxide

1 reference

12 December 2020

Construction of substituted N-hydroxyindoles: synthesis of a nocathiacin I model system

1 reference

12 December 2020

10.1016/J.TET.2007.03.072

Identifiers

DOI

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30 July 2017

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30 July 2017

1 reference