(Q24681238)

English

Total synthesis of kendomycin: a macro-C-glycosidation approach

scientific article

In more languages

default for all languages

No label defined

No description defined

edit

Statements

instance of

scholarly article

0 references

title

Total synthesis of kendomycin: a macro-C-glycosidation approach (English)

0 references

0 references

Yu Yuan

1

0 references

Hongbin Men

series ordinal

2

0 references

Chulbom Lee

series ordinal

3

0 references

publication date

17 November 2004

0 references

language of work or name

English

0 references

published in

Journal of the American Chemical Society

0 references

volume

126

0 references

issue

45

0 references

page(s)

14720-1

0 references

cites work

Regioselective oxidation of phenols to o-quinones with o-iodoxybenzoic acid (IBX)

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785127

retrieved

7 April 2017

Toward the synthesis of the carbacylic ansa antibiotic kendomycin.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785127

retrieved

28 September 2017

Synthetic approach to kendomycin: preparation of the C-glycosidic core

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785127

retrieved

28 November 2018

Asymmetric Synthesis of Phorboxazole B-Part I: Synthesis of the C(20)-C(38) and C(39)-C(46) Subunits Financial support was provided by the National Institutes of Health (GM-33328) and the National Science Foundation. An American Cancer Society Postd

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15535687

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthetic Cyclic Oligosaccharides

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15535687

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthetic Studies on Borrelidin: Enantioselective Synthesis of the C1−C12 Fragment

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15535687

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A stabilized formulation of IBX (SIBX) for safe oxidation reactions including a new oxidative demethylation of phenolic methyl aryl ethers

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15535687

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel approach toward the synthesis of kendomycin: selective synthesis of a C-aryl glycoside as a single atropisomer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15535687

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of the C1-C13 Fragment of Kendomycin: Atropisomerism around a C-Aryl Glycosidic Bond

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15535687

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

0 references

0 references

PubMed publication ID

15535687

0 references

ResearchGate publication ID

51367054

0 references

(Q24681238)

Total synthesis of kendomycin: a macro-C-glycosidation approach

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)