(Q34686853)

3 August 2017

Total synthesis of (+)-dactylolide. (English)

1 reference

3 August 2017

Carina C Sanchez

1

1 reference

PubMed ID

15987203

3 August 2017

Gary E Keck

series ordinal

2

1 reference

PubMed ID

15987203

3 August 2017

language of work or name

English

0 references

publication date

1 July 2005

1 reference

3 August 2017

1 reference

3 August 2017

7

1 reference

3 August 2017

14

1 reference

3 August 2017

3053-3056

1 reference

Pyran annulation: asymmetric synthesis of 2,6-disubstituted-4-methylene tetrahydropyrans

3 August 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1480405

Macrolactonization via Ti(IV)-mediated epoxy-acid coupling: a total synthesis of (-)-dactylolide [and zampanolide].

7 July 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1480405

Total synthesis of (+)-zampanolide

26 October 2018

1 reference

12 December 2020

Total synthesis of (+)-dactylolide

1 reference

12 December 2020

Catalytic asymmetric allylation reactions using BITIP catalysis and 2-substituted allylstannanes as surrogates for beta-keto ester dianions

1 reference

12 December 2020

An expedient total synthesis of (-)-dactylolide and formal synthesis of (-)-zampanolide

1 reference

12 December 2020

Total synthesis of (+)-dactylolide through an efficient sequential Peterson olefination and Prins cyclization reaction

1 reference

12 December 2020

Diastereoselective synthesis of the C(17)-C(28) fragment (the C-D spiroketal unit) of spongistatin 1 (altohyrtin A) via a kinetically controlled iodo-spiroketalization reaction

1 reference

12 December 2020

Dactylolide, a New Cytotoxic Macrolide from the Vanuatu SpongeDactylospongia sp.

0 references

Identifiers

DOI

10.1021/OL051040G

1 reference

3 August 2017

1 reference

3 August 2017

1 reference

PubMed ID

15987203