(Q39815422)

14 September 2017

Total synthesis and structure-activity investigation of the marine natural product neopeltolide (English)

1 reference

14 September 2017

marine natural product

0 references

1 reference

5

1 reference

14 September 2017

Daniel W Custar

1

1 reference

14 September 2017

Thomas P Zabawa

series ordinal

2

1 reference

14 September 2017

John Hines

series ordinal

3

1 reference

14 September 2017

Craig M Crews

series ordinal

4

1 reference

14 September 2017

language of work or name

English

0 references

publication date

1 September 2009

1 reference

Journal of the American Chemical Society

14 September 2017

1 reference

14 September 2017

131

1 reference

14 September 2017

34

1 reference

14 September 2017

12406-12414

1 reference

Oxidative carbocation formation in macrocycles: synthesis of the neopeltolide macrocycle

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Dual macrolactonization/pyran-hemiketal formation via acylketenes: applications to the synthesis of (-)-callipeltoside A and a lyngbyaloside B model system

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Total synthesis and biological activity of neopeltolide and analogues

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Formal synthesis of (-)-kendomycin featuring a Prins-cyclization to construct the macrocycle

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Synthesis enables identification of the cellular target of leucascandrolide A and neopeltolide

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Efficient synthetic access to a new family of highly potent bryostatin analogues via a Prins-driven macrocyclization strategy

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Total synthesis and stereochemical reassignment of (+)-neopeltolide

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Racemization in Prins cyclization reactions

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Marine natural products and related compounds in clinical and advanced preclinical trials

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Advanced preclinical and clinical trials of natural products and related compounds from marine sources

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Natural products as sources of new drugs over the period 1981-2002.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Concise enantioselective total synthesis of neopeltolide macrolactone highlighted by ether transfer.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Total synthesis of the marine macrolide (+)-neopeltolide

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Total synthesis and structural revision of the marine macrolide neopeltolide

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Lyngbouilloside, a novel glycosidic macrolide from the marine cyanobacterium Lyngbya bouillonii

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Total Synthesis of (+)-Neopeltolide

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735232

Neopeltolide, a macrolide from a lithistid sponge of the family Neopeltidae

2 December 2018

1 reference

12 December 2020

Lyngbyaloside B, a new glycoside macrolide from a Palauan marine cyanobacterium, Lyngbya sp

1 reference

12 December 2020

Role of 2-oxonia Cope rearrangements in Prins cyclization reactions

1 reference

12 December 2020

Stereocontrolled and convergent total synthesis of amphidinolide T3

1 reference

12 December 2020

Synthesis of leucascandrolide A via a spontaneous macrolactolization

1 reference

12 December 2020

Total synthesis of (+)-neopeltolide by a Prins macrocyclization

1 reference

12 December 2020

Aurisides A and B, Cytotoxic Macrolide Glycosides from the Japanese Sea HareDolabella auricularia

1 reference

12 December 2020

The Vinylogous Aldol Reaction: A Valuable, Yet Understated Carbon−Carbon Bond-Forming Maneuver

1 reference

12 December 2020

Synthesis of functionalized oxazolines and oxazoles with DAST and Deoxo-Fluor

1 reference

12 December 2020

Formal total synthesis of neopeltolide

1 reference

12 December 2020

Stereoselective synthesis of tetrahydropyran-4-ones from dioxinones catalyzed by scandium(III) triflate

1 reference

12 December 2020

Leucascandrolide A, a New Type of Macrolide: The first powerfully bioactive metabolite of calcareous sponges (Leucascandra caveolata, a new genus from the coral sea)

1 reference

9 March 2024

https://opencitations.net/index/api/v1/citations/10.1002/HLCA.19960790107

Identifiers

DOI

10.1021/JA904604X

1 reference

14 September 2017

1 reference

14 September 2017

PubMed publication ID

19663512

1 reference