(Q35580559)

English

Study on the biosynthesis of the notoamides: Pinacol-type rearrangement of the isoprenyl unit in deoxybrevianamide E and 6-hydroxydeoxybrevianamide E.

scientific article published on December 2011

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scholarly article

1 reference

Europe PubMed Central

9 August 2017

Study on the biosynthesis of the notoamides: Pinacol-type rearrangement of the isoprenyl unit in deoxybrevianamide E and 6-hydroxydeoxybrevianamide E. (English)

1 reference

Europe PubMed Central

9 August 2017

deoxybrevianamide e

1 reference

ChEBI release 2020-05-28

corrigendum / erratum

Corrigendum to “Study on the biosynthesis of the notoamides: pinacol-type rearrangement of the isoprenyl unit in deoxybrevianamide E and 6-hydroxydeoxybrevianamide E” [Tetrahedron Lett. 52 (2011) 6923–6926]

1 reference

10.1016/J.TETLET.2013.11.076

12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1016/J.TETLET.2013.11.076

Sachiko Tsukamoto

object named as

Sachiko Tsukamoto

7

0 references

author name string

Hikaru Kato

1

1 reference

Europe PubMed Central

9 August 2017

Yuichi Nakamura

2

1 reference

Europe PubMed Central

9 August 2017

Jennifer M Finefield

3

1 reference

Europe PubMed Central

9 August 2017

Hideharu Umaoka

4

1 reference

Europe PubMed Central

9 August 2017

Takashi Nakahara

5

1 reference

Europe PubMed Central

9 August 2017

Robert M Williams

6

1 reference

Europe PubMed Central

9 August 2017

publication date

1 December 2011

1 reference

Europe PubMed Central

9 August 2017

Tetrahedron Letters

1 reference

Europe PubMed Central

9 August 2017

52

1 reference

Europe PubMed Central

9 August 2017

6923-6926

1 reference

Europe PubMed Central

9 August 2017

51

1 reference

Europe PubMed Central

9 August 2017

Studies on the biosynthesis of the notoamides: synthesis of an isotopomer of 6-hydroxydeoxybrevianamide E and biosynthetic incorporation into notoamide J.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226720

12 July 2018

Notoamide O, a structurally unprecedented prenylated indole alkaloid, and notoamides P-R from a marine-derived fungus, Aspergillus sp.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226720

12 July 2018

Asymmetric total syntheses of (+)- and (-)-versicolamide B and biosynthetic implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226720

12 July 2018

Isolation of notoamide E, a key precursor in the biosynthesis of prenylated indole alkaloids in a marine-derived fungus, Aspergillus sp

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226720

12 July 2018

Isolation of antipodal (-)-versicolamide B and notoamides L-N from a marine-derived Aspergillus sp.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226720

12 July 2018

Isolation, structure elucidation, and biomimetic total synthesis of versicolamide B, and the isolation of antipodal (-)-stephacidin A and (+)-notoamide B from Aspergillus versicolor NRRL 35600.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226720

12 July 2018

Stephacidin A and B: two structurally novel, selective inhibitors of the testosterone-dependent prostate LNCaP cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226720

12 July 2018

Novel antinematodal and antiparasitic agents from Penicillium charlesii. II. Structure determination of paraherquamides B, C, D, E, F, and G.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226720

12 July 2018

Novel antinematodal and antiparasitic agents from Penicillium charlesii. I. Fermentation, isolation and biological activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226720

12 July 2018

Notoamides F-K, prenylated indole alkaloids isolated from a marine-derived Aspergillus sp.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226720

26 September 2018

Malbrancheamide B, a novel compound from the fungus Malbranchea aurantiaca.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226720

26 September 2018

Novel anthelmintic metabolites from an Aspergillus species; the aspergillimides

1 reference

https://pubmed.ncbi.nlm.nih.gov/22140281

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Concise Total Synthesis of the Notoamides C and D

1 reference

https://pubmed.ncbi.nlm.nih.gov/22140281

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine-Derived Fungus,Aspergillus sp

1 reference

https://pubmed.ncbi.nlm.nih.gov/22140281

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B

1 reference

https://pubmed.ncbi.nlm.nih.gov/22140281

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies in relation to biosynthesis. XLII. The structural elucidation and some aspects of the biosynthesis of the brevianamides-A and -E

1 reference

https://pubmed.ncbi.nlm.nih.gov/22140281

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.TETLET.2011.10.065

1 reference

Europe PubMed Central

9 August 2017

1 reference

Europe PubMed Central

9 August 2017

1 reference

Europe PubMed Central

9 August 2017

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