(Q42136551)

17 October 2017

Total synthesis of (+)-batzelladine A and (-)-batzelladine D via [4 + 2]-annulation of vinyl carbodiimides with N-alkyl imines (English)

1 reference

17 October 2017

Michael A Arnold

1

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author name string

Kenneth A Day

series ordinal

2

1 reference

17 October 2017

Sergio G Durón

series ordinal

3

1 reference

17 October 2017

David Y Gin

series ordinal

4

1 reference

17 October 2017

language of work or name

English

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publication date

1 October 2006

1 reference

Journal of the American Chemical Society

17 October 2017

1 reference

17 October 2017

128

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17 October 2017

40

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17 October 2017

13255-13260

1 reference

Enantioselective total synthesis of batzelladine F and definition of its structure.

17 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2610335

Evolution of a strategy for the synthesis of structurally complex batzelladine alkaloids. Enantioselective total synthesis of the proposed structure of batzelladine F and structural revision

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2610335

Asymmetric total synthesis of batzelladine D.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2610335

Synthesis and activity of a new generation of ruthenium-based olefin metathesis catalysts coordinated with 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene ligands

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2610335

Total synthesis of (+)-batzelladine A and (-)-batzelladine D, and identification of their target protein.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2610335

Diastereoselective [4+2] annulation of vinyl carbodiimides with N-alkyl imines. Asymmetric synthetic access to the batzelladine alkaloids

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2610335

Studies towards the total synthesis of batzelladine A.

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2610335

Synthesis of the phosphoramidite derivatives of 2'-deoxy-2'-C-alpha-methylcytidine and 2'-deoxy-2'-C-alpha-hydroxymethylcytidine: analogues for chemical dissection of RNA's 2'-hydroxyl group

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2610335

Application of the Tethered Biginelli Reaction for Enantioselective Synthesis of Batzelladine Alkaloids. Absolute Configuration of the Tricyclic Guanidine Portion of Batzelladine B.

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2610335

Enantioselective total synthesis of batzelladine F: structural revision and stereochemical definition

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2610335

Synthesis of (+/-)-phloeodictine A1.

17 August 2018

1 reference

12 December 2020

Revision of the stereochemistry of batzelladine F. Approaches to the tricyclic hydroxyguanidine moiety of batzelladines G, H, and I

1 reference

12 December 2020

Total synthesis of batzelladine D

1 reference

12 December 2020

Reduction of Secondary Carboxamides to Imines

1 reference

12 December 2020

Novel polycyclic guanidine alkaloids from two marine sponges of the genus Monanchora

1 reference

12 December 2020

Enantioselective Total Synthesis of Batzelladine A

1 reference

12 December 2020

Synthesis and determination of absolute configuration of the bicyclic guanidine core of batzelladine A

1 reference

12 December 2020

Identifiers

DOI

10.1021/JA063860+

1 reference

17 October 2017

1 reference

17 October 2017

1 reference