(Q37265454)

19 August 2017

Spongipyran Synthetic Studies. Total Synthesis of (+)-Spongistatin 2. (English)

1 reference

19 August 2017

Amos B Smith

1

1 reference

19 August 2017

Qiyan Lin

2

1 reference

19 August 2017

Victoria A Doughty

3

1 reference

19 August 2017

Linghang Zhuang

4

1 reference

19 August 2017

Mark D McBriar

5

1 reference

19 August 2017

Jeffrey K Kerns

6

1 reference

19 August 2017

Armen M Boldi

7

1 reference

19 August 2017

Noriaki Murase

8

1 reference

19 August 2017

William H Moser

9

1 reference

19 August 2017

Christopher S Brook

10

1 reference

19 August 2017

Clay S Bennett

11

1 reference

19 August 2017

Kiyoshi Nakayama

12

1 reference

19 August 2017

Masao Sobukawa

13

1 reference

19 August 2017

Robert E Lee Trout

14

1 reference

19 August 2017

1 August 2009

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19 August 2017

1 reference

19 August 2017

65

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19 August 2017

33

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19 August 2017

6470-6488

1 reference

Ortho-TMS benzaldehyde: an effective linchpin for type II anion relay chemistry (ARC).

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

Anion relay chemistry: an effective tactic for diversity oriented synthesis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

Total synthesis of (+)-spongistatin 1. An effective second-generation construction of an advanced EF Wittig salt, fragment union, and final elaboration

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

Synthesis of the C29-C44 portion of spongistatin 1 (altohyrtin A).

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

A broad-spectrum antifungal from the marine sponge Hyrtios erecta

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

Multicomponent linchpin couplings. Reaction of dithiane anions with terminal epoxides, epichlorohydrin, and vinyl epoxides: efficient, rapid, and stereocontrolled assembly of advanced fragments for complex molecule synthesis

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

Multigram synthesis of the C29-C51 subunit and completion of the total synthesis of altohyrtin C (spongistatin 2).

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

A Second-Generation Synthesis of the C1−C28 Portion of the Altohyrtins (Spongistatins)

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

Total synthesis of (+)-phorboxazole A exploiting the Petasis-Ferrier rearrangement

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

Synthesis of the C1-C28 Portion of Spongistatin 1 (Altohyrtin A).

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

A Method for Constructing the C18-C28 Dispiroacetal Moiety of Altohyrtin A.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

A Method for Constructing the C2-C12 Dispiroacetal Moiety of Altohyrtin A.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

The regioselectivity of addition of organolithium reagents to enones and enals: the role of HMPA.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

Synthesis of a C(29)-C(51) subunit of spongistatin 1 (Altohyrtin A) starting from (R)-3-benzyloxy-2-methylpropan-1-ol

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

The [1,5]-Brook Rearrangement: An Initial Application in Anion Relay Chemistry

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo-Symmetry

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

Synthesis of the C-1−C-28 ABCD Unit of Spongistatin 1

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2712115

Synthesis of the C16-C28 spiroketal subunit of spongistatin 1 (altohyrtin A): the pyrone approach

3 December 2018

1 reference

12 December 2020

Bidirectional asymmetric allylboration. A convenient asymmetric synthesis of C(2)-symmetric 3-methylenepentane-1,5-diols and rapid access to C(2)-symmetric spiroketals

1 reference

12 December 2020

A modular approach to marine macrolide construction. 3. Enantioselective synthesis of the C1-C28 sector of spongistatin 1 (altohyrtin A)

1 reference

12 December 2020

Synthesis of the C(29)-C(45) bis-pyran subunit (E-F) of spongistatin 1 (Altohyrtin A)

1 reference

12 December 2020

The Spongistatins: Architecturally Complex Natural Products-Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment Financial support was provided by the National Institutes of Health (National Cancer Institut

1 reference

12 December 2020

Spongistatin synthetic studies. An efficient, second-generation construction of an advanced ABCD intermediate

1 reference

12 December 2020

Asymmetric total synthesis of spongistatins 1 and 2

1 reference

12 December 2020

Chiral synthesis via organoboranes. 7. Diastereoselective and enantioselective synthesis of erythro- and threo-.beta.-methylhomoallyl alcohols via enantiomeric (Z)- and (E)-crotylboranes

1 reference

12 December 2020

The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2

1 reference

12 December 2020

Stereocontrolled Total Synthesis of (+)-Altohyrtin A/Spongistatin 1 Financial support was provided by the EPSRC (GR/L41646), Cambridge Commonwealth Trust (Scholarship to M.J.C.), EC (Marie Curie Postdoctoral Fellowship to J.L.A.), DFG (Postdoctoral

1 reference

12 December 2020

The spongistatins, potently cytotoxic inhibitors of tubulin polymerization, bind in a distinct region of the vinca domain

1 reference

12 December 2020

Altohyrtins B and C and 5-desacetylaltohyrtin A, potent cytotoxic macrolide congeners of altohyrtin A, from the Okinawan marine sponge Hyrtios altum

1 reference

12 December 2020

Synthesis and in vitro cancer cell growth inhibitory activity of monocyclic model compounds containing spongistatin triene side-chains

1 reference

12 December 2020

Asymmetric synthesis using diisopropyl tartrate modified (E)- and (Z)-crotylboronates: preparation of the chiral crotylboronates and reactions with achiral aldehydes

1 reference

19 October 2022

https://opencitations.net/index/coci/api/v1/citations/10.1021/JA00173A023

Identifiers

DOI

10.1016/J.TET.2009.04.001

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

20161196

1 reference