(Q64990704)

English

Asymmetric Total Synthesis of the Gastroprotective Microbial Agent AI-77-B.

scientific article published on 10 February 2003

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

Asymmetric Total Synthesis of the Gastroprotective Microbial Agent AI-77-B. (English)

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

author name string

Arun K Ghosh

1

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

Alexander Bischoff

2

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

John Cappiello

3

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

publication date

10 February 2003

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

European Journal of Organic Chemistry

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

2003

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

5

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

821-832

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

1H-2-Benzopyran-1-one derivatives, microbial products with pharmacological activity. Conversion into orally active derivatives with antiinflammatory and antiulcer activities

1 reference

https://pubmed.ncbi.nlm.nih.gov/30393460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diphenylphosphoryl azide. A new convenient reagent for a modified Curtus reaction and for the peptide synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/30393460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1H-2-benzopyran-1-one derivatives, microbial products with pharmacological activity. Relationship between structure and activity in 6-[[1(S)-(3(S),4- dihydro-8-hydroxy-1-oxo-1H-2-benzopyran-3-yl)-3-methylbutyl]-amino]-4(S), 5(S)-dihydroxy-6-oxo-3(S)

1 reference

https://pubmed.ncbi.nlm.nih.gov/30393460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stereoselective synthesis of pseudopeptide microbial agent AI-77-B

1 reference

https://pubmed.ncbi.nlm.nih.gov/30393460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asymmetric Synthesis of the Dihydroisocoumarin Moiety of AI-77-B via Copper-Mediated Cross-Coupling and Sharpless Asymmetric Dihydroxylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/30393460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total Synthesis of (+)-Sinefungin

1 reference

https://pubmed.ncbi.nlm.nih.gov/30393460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Practical Method for the Removal of Organotin Residues from Reaction Mixtures

1 reference

https://pubmed.ncbi.nlm.nih.gov/30393460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transition-State Mimetics for HIV Protease Inhibitors: Stereocontrolled Synthesis of Hydroxyethylene and Hydroxyethylamine Isosteres by Ester-Derived Titanium Enolate Syn and Anti-Aldol Reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/30393460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/EJOC.200390125

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6214212

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