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Enantiopure 1,5-diols from dynamic kinetic asymmetric transformation. Useful synthetic intermediates for the preparation of chiral heterocycles
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description
wetenschappelijk artikel
(nl)
наукова стаття, опублікована в травні 2008
(uk)
im Mai 2008 veröffentlichter wissenschaftlicher Artikel
(de)
publication date
wds:Q56949836-47009157-BD99-4AC4-B09E-7D376BDF915E
publication date
2008-05-15 00:00:00Z
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language of work or name
wds:Q56949836-BBFF9A78-CFB4-4155-A8C5-9C084CAD0F95
language of work or name
English
author name string
wds:Q56949836-2683BA96-E315-419F-8A6F-E2CCC156972F
wds:Q56949836-2DE596C8-01E4-4681-94D7-E682FE9EF8E8
wds:Q56949836-75B9D826-DA33-4D2B-97C4-B911B0CBBC9B
author name string
Linnéa Borén
Karin Leijondahl
Roland Braun
rdfs:label
Enantiopure 1,5-diols from dynamic kinetic asymmetric transformation. Useful synthetic intermediates for the preparation of chiral heterocycles
(en)
Enantiopure 1,5-diols from dynamic kinetic asymmetric transformation. Useful synthetic intermediates for the preparation of chiral heterocycles
(nl)
skos:prefLabel
Enantiopure 1,5-diols from dynamic kinetic asymmetric transformation. Useful synthetic intermediates for the preparation of chiral heterocycles
(en)
Enantiopure 1,5-diols from dynamic kinetic asymmetric transformation. Useful synthetic intermediates for the preparation of chiral heterocycles
(nl)
name
Enantiopure 1,5-diols from dynamic kinetic asymmetric transformation. Useful synthetic intermediates for the preparation of chiral heterocycles
(en)
Enantiopure 1,5-diols from dynamic kinetic asymmetric transformation. Useful synthetic intermediates for the preparation of chiral heterocycles
(nl)
author
wds:Q56949836-66EABE04-0AA8-4936-B7A3-B04909870621
author
Jan-Erling Bäckvall
title
wds:Q56949836-BCCCB6A1-313D-488A-93DE-7E76FB959FC7
title
Enantiopure 1,5-diols from dynamic kinetic asymmetric transformation. Useful synthetic intermediates for the preparation of chiral heterocycles
(en)
page(s)
wds:Q56949836-BAD162AD-51C6-4DFC-B902-FA7D2D94AF0B
page(s)
2027-30
instance of
wds:Q56949836-6771138A-8C52-47F4-A479-005AD7150EBB
instance of
scholarly article
main subject
wds:Q56949836-47A931FA-7779-453F-B8BC-DA253770381D
main subject
chirality
PubMed ID
wds:Q56949836-F3BD1E49-9B6F-4CF4-8142-C0275A2AB0F6
PubMed ID
http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18402460
PubMed ID
18402460
published in
wds:Q56949836-D5BCBA73-D9C3-4A64-835B-6DD779260535
published in
Organic Letters
issue
wds:Q56949836-99B8B765-EBC9-4098-AA74-3AC81518138F
volume
wds:Q56949836-96A8CE4F-6303-4674-B510-F174D5FB30FC
issue
10
volume
10
DOI
wds:Q56949836-93F76C59-015A-4298-B7AE-DC2A69B0A914
DOI
http://dx.doi.org/10.1021/OL800468H
DOI
10.1021/OL800468H
is
about
of
https://www.wikidata.org/wiki/Special:EntityData/Q56949836
is
cites work
of
New strategy for the synthesis of substituted morpholines
Chemoenzymatic dynamic kinetic resolution: a powerful tool for the preparation of enantiomerically pure alcohols and amines.
Asymmetric synthesis of bicyclic diol derivatives through metal and enzyme catalysis: application to the formal synthesis of sertraline
Heterocycles via intramolecular platinum-catalyzed propargylic substitution
Stereoselective synthesis of 2,5-disubstituted morpholines using a palladium-catalyzed hydroamination reaction
The first stereoselective total synthesis of neosemburin and isoneosemburin.
is
cites work
of
wds:Q43094737-44D88E88-80CC-44D6-8057-4BA4BB1AC1C4
wds:Q41862367-5D79AD1F-76BC-408D-911A-B52EACF68F4B
wds:Q57991541-FCDF349B-A91E-4AD8-86B8-396552A8CA66
wds:Q38366683-67A943FB-677C-4A46-B066-94F21F204A09
wds:Q43145190-6C440315-0654-42C4-B46F-C9E6806EC130
wds:Q47836538-E1518635-E259-4DA3-9E19-C7F53883E039
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