(Q58134934)

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STEREOSELECTIVE REDUCTION OF α-HYDROXY OXIME ETHERS: A CONVENIENT ROUTE TO CIS-1,2-AMINO ALCOHOLS

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STEREOSELECTIVE REDUCTION OF α-HYDROXY OXIME ETHERS: A CONVENIENT ROUTE TO CIS-1,2-AMINO ALCOHOLS (English)

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Arun K Ghosh

1

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Sean P Mckee

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2

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Wilham M Sanders

series ordinal

3

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language of work or name

English

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publication date

4 February 1991

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published in

Tetrahedron Letters

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volume

32

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issue

6

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page(s)

711-714

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cites work

Confirmation by synthesis of the structure of acosamine and methyl N-acetylactinosaminide

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6200347

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30 November 2018

Stereochemical studies of adrenergic drugs. Diastereomeric 2-amino-1-phenylcyclobutanols

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https://api.crossref.org/works/10.1016%2FS0040-4039%2800%2974864-7

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Addition of iodine isocyanate to olefins. Scope and synthetic utility

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m-Chloroperbenzoic acid oxidation of 2-trimethylsilyloxy-1,3-dienes. Synthesis of .alpha.-hydroxy and .alpha.-acetoxy enones

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Synthetic methods. VIII. Hydroxylation of carbonyl compounds via silyl enol ethers

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Protection of hydroxyl groups as tert-butyldimethylsilyl derivatives

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DOI

10.1016/S0040-4039(00)74864-7

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PMC publication ID

6200347

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PubMed publication ID

30369641

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(Q58134934)

STEREOSELECTIVE REDUCTION OF α-HYDROXY OXIME ETHERS: A CONVENIENT ROUTE TO CIS-1,2-AMINO ALCOHOLS

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