(Q37230627)

English

Evolution of the total synthesis of (-)-okilactomycin exploiting a tandem oxy-cope rearrangement/oxidation, a Petasis-Ferrier union/rearrangement, and ring-closing metathesis

scientific article published on February 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Evolution of the total synthesis of (-)-okilactomycin exploiting a tandem oxy-cope rearrangement/oxidation, a Petasis-Ferrier union/rearrangement, and ring-closing metathesis (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

author name string

Amos B Smith

1

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Todd Bosanac

2

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Kallol Basu

3

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

language of work or name

0 references

publication date

1 February 2009

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Journal of the American Chemical Society

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

131

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

2348-2358

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Macrocyclization by Ring-Closing Metathesis in the Total Synthesis of Natural Products: Reaction Conditions and Limitations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697663

6 September 2017

A cyclopropane fragmentation approach to heterocycle assembly: a convergent synthesis of oxepanes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697663

6 September 2017

Evolution of the Petasis-Ferrier union/rearrangement tactic: construction of architecturally complex natural products possessing the ubiquitous cis-2,6-substituted tetrahydropyran structural element

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697663

3 September 2018

Total synthesis of the marine natural product (-)-clavosolide A. A showcase for the Petasis-Ferrier union/rearrangement tactic.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697663

3 September 2018

Synthesis and evaluation of 3-(carboxymethylidene)- and 3-(carboxymethyl)penicillinates as inhibitors of beta-lactamase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697663

3 September 2018

Total synthesis of (-)-kendomycin exploiting a Petasis-Ferrier rearrangement/ring-closing olefin metathesis synthetic strategy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697663

3 September 2018

General Approach for the Synthesis of Sarpagine Indole Alkaloids. Enantiospecific Total Synthesis of (+)-Vellosimine, (+)-Normacusine B, (−)-Alkaloid Q3, (−)-Panarine, (+)-Na-Methylvellosimine, and (+)-Na-Methyl-16-epipericyclivine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697663

3 September 2018

Convenient Preparation of Cyclic Acetals, Using Diols, TMS-Source, and a Catalytic Amount of TMSOTf

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697663

3 September 2018

Total synthesis of (+)-phorboxazole A exploiting the Petasis-Ferrier rearrangement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697663

3 September 2018

Okilactomycin, a novel antibiotic produced by a Streptomyces species. I. Taxonomy, fermentation, isolation and characterization.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697663

3 September 2018

Phorboxazole synthetic studies. 1. Construction of a C(3-19) subtarget exploiting an extension of the Petasis-Ferrier rearrangement

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phorboxazole synthetic studies. 2. Construction of a C(20-28) subtarget, a further extension of the Petasis-Ferrier rearrangement

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chrolactomycin, a novel antitumor antibiotic produced by Streptomyces sp

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthetic studies toward bioactive cyclic peroxides from the marine sponge Plakortis angulospiculatus

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total syntheses of (+)-zampanolide and (+)-dactylolide exploiting a unified strategy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective preparation of the C1-C11 fragment of apoptolidin

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spongistatin synthetic studies. evolution of a scalable synthesis for the EF fragment of (+)-Spongistatin 1 exploiting a Petasis-Ferrier union/rearrangement tactic

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthetic studies toward highly functionalized 5beta-lanosterol derivatives: a versatile approach utilizing anionic cycloaddition

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total synthesis of (-)-okilactomycin

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Palladium-catalyzed formylation of organic halides with carbon monoxide and tin hydride

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biosynthesis of the antibiotic okilactomycin

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Okilactomycin, a novel antibiotic produced by a Streptomyces species. II. Structure determination

1 reference

https://pubmed.ncbi.nlm.nih.gov/19170499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA8084669

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

ResearchGate publication ID

0 references

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