(Q24648995)

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Asymmetric synthesis of diastereomeric diaminoheptanetetraols. A proposal for the configuration of (+)-zwittermicin a

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Asymmetric synthesis of diastereomeric diaminoheptanetetraols. A proposal for the configuration of (+)-zwittermicin a (English)

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2

Tadeusz F Molinski

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author name string

Evan W Rogers

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1

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language of work or name

English

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publication date

1 February 2007

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published in

Organic Letters

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volume

9

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issue

3

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page(s)

437-40

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cites work

Genetics of zwittermicin a production by Bacillus cereus

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PubMed Central

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7 April 2017

Zwittermicin A biosynthetic cluster

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PubMed Central

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28 September 2017

ZmaR, a novel and widespread antibiotic resistance determinant that acetylates zwittermicin A.

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2729442

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28 September 2017

Biological activities of two fungistatic antibiotics produced by Bacillus cereus UW85

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PubMed Central

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28 September 2017

The C2 selective nucleophilic substitution reactions of 2,3-epoxy alcohols mediated by trialkyl borates: the first endo-mode epoxide-opening reaction through an intramolecular metal chelate.

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PubMed Central

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retrieved

28 November 2018

Enantiopure preparation of the two enantiomers of the pseudo-C(2)-symmetric N,N-dibenzyl-1,2:4,5-diepoxypentan-3-amine

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2729442

retrieved

28 November 2018

Target range of zwittermicin A, an aminopolyol antibiotic from Bacillus cereus

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17249781

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12 December 2020

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Stereochemical Determination of Acyclic Structures Based on Carbon-Proton Spin-Coupling Constants. A Method of Configuration Analysis for Natural Products

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17249781

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12 December 2020

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PubMed publication ID

17249781

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ResearchGate publication ID

6553453

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(Q24648995)

Asymmetric synthesis of diastereomeric diaminoheptanetetraols. A proposal for the configuration of (+)-zwittermicin a

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