(Q41899975)

English

An expedient formal total synthesis of (-)-diazonamide A via a powerful, stereoselective O-aryl to C-aryl migration to form the C10 quaternary center

scientific article published on 19 September 2007

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

An expedient formal total synthesis of (-)-diazonamide A via a powerful, stereoselective O-aryl to C-aryl migration to form the C10 quaternary center (English)

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

stereoselectivity

1 reference

based on heuristic

inferred from title

author name string

Chi-Ming Cheung

1

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Frederick W Goldberg

2

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Philip Magnus

3

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Claire J Russell

4

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Rachel Turnbull

5

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Vince Lynch

6

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

language of work or name

0 references

publication date

19 September 2007

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Journal of the American Chemical Society

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

129

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

40

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

12320-12327

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Chemistry and biology of diazonamide A: second total synthesis and biological investigations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

5 June 2018

Chemistry and biology of diazonamide A: first total synthesis and confirmation of the true structure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

5 June 2018

A Concise and Flexible Total Synthesis of (−)‐Diazonamide A

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

5 June 2018

The Second Total Synthesis of Diazonamide A

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

5 June 2018

Total Synthesis of Nominal Diazonamides-Part 2: On the True Structure and Origin of Natural Isolates Funding provided by the NIH (RO1-GM60591), the NSF (CAREER 9984282), the Howard Hughes Medical Institute (junior faculty support), the Robert A. Wel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

5 June 2018

Total Synthesis of Nominal Diazonamides-Part 1: Convergent Preparation of the Structure Proposed for (-)-Diazonamide A Funding provided by the NIH (RO1-GM60591), the NSF (CAREER 9984282), the Howard Hughes Medical Institute (junior faculty support),

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

5 June 2018

Total synthesis of diazonamide A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

5 June 2018

Approaches to the quaternary stereocentre and to the heterocyclic core in diazonamide A using the Heck reaction and related coupling reactions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

18 August 2018

The diazo route to diazonamide A: studies on the tyrosine-derived fragment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

18 August 2018

The diazo route to diazonamide A. Studies on the indole bis-oxazole fragment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

18 August 2018

Indol-2-one intermediates: mechanistic evidence and synthetic utility. Total syntheses of (+/-)-flustramines A and C.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

18 August 2018

Studies toward diazonamide A: development of a hetero-pinacol macrocyclization cascade for the construction of the bis-macrocyclic framework of the originally proposed structure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

18 August 2018

Studies toward diazonamide A: initial synthetic forays directed toward the originally proposed structure.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

18 August 2018

Diazonamide synthesis studies: use of Negishi coupling to fashion diazonamide-related biaryls with defined axial chirality.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

18 August 2018

Model Studies towards Diazonamide A: Synthesis of the Heterocyclic Core We thank Dr. D. H. Huang, Dr. G. Suizdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. We also thank Profess

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536501

18 August 2018

Stereocontrol in Pinacol Ring-Contraction of Cyclopeptidyl Glycols: The Diazonamide C(10) Problem We thank Mr. Imran Alibhai and Dr. Jing Li for invaluable experimental assistance. Financial support provided by the Advanced Research Program of the T

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A tyrosine-derived benzofuranone related to diazonamide A

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progress toward synthesis of diazonamide A. Preparation of a 3-(oxazol-5-yl)-4-trifluoromethyl-sulfonyloxyindole and its use in biaryl coupling reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of C(3) benzofuran-derived bisaryl quaternary centers: approaches to diazonamide A

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthetic studies toward diazonamide A. A novel approach for polyoxazole synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of the diazonamide A macrocyclic core via a Dieckmann-type cyclization

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total Synthesis of Bistratamide D

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The diazonamides: the plot thickens

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stereodirected synthesis of aryl alpha-C-glycosides from 2-O-arylsilyl-glucopyranosides

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A synthesis of the diazonamide heteroaromatic biaryl macrocycle/hemiaminal core

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total synthesis of (+/-)-perophoramidine

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mild thermal and acid-catalyzed rearrangement of O-aryl ethers into ortho-hydroxy arenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biomimetic approaches to diazonamide A. Direct synthesis of the indole bis-oxazole fragment by oxidation of a TyrValTrpTrp tetrapeptide

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The remarkable effect of the 7-substituent in the diastereoselective oxidative rearrangement of indoles: Asymmetric synthesis of 3,3-disubstituted oxindoles

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oxidative Rearrangement of Indoles: A New Approach to the EFHG-Tetracyclic Core of Diazonamide A

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthetic seco Forms of (-)-Diazonamide A.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17880079

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of heterocyclic natural products: Model studies towards diazonamide A

1 reference

20 August 2023

https://opencitations.net/index/coci/api/v1/citations/10.1351/PAC199466102107

Identifiers

10.1021/JA0744448

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

ResearchGate publication ID

0 references

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