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Proline-catalysed Mannich reactions of acetaldehyde.
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Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
title
Proline-catalysed Mannich reactions of acetaldehyde
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
author
Jung Woon Yang
series ordinal
1
1 reference
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Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
Benjamin List
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5
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Benjamin List
1 reference
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Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
author name string
Carley Chandler
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2
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Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
Michael Stadler
series ordinal
3
1 reference
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Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
Daniela Kampen
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
language of work or name
English
0 references
publication date
20 February 2008
1 reference
stated in
Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
published in
Nature
1 reference
stated in
Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
volume
452
1 reference
stated in
Europe PubMed Central
PubMed ID
18288105
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
issue
7186
1 reference
stated in
Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
page(s)
453-455
1 reference
stated in
Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
exact match
https://scigraph.springernature.com/pub.10.1038/nature06740
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Chemistry. The organic approach to asymmetric catalysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06740
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7 January 2021
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Asymmetric enamine catalysis
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https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
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Proline-catalyzed one-step asymmetric synthesis of 5-hydroxy-(2E)-hexenal from acetaldehyde.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Direct catalytic asymmetric aldol reactions of aldehydes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
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inferred from DOI database lookup
The Catalytic Asymmetric Aldol Reaction.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
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inferred from DOI database lookup
Lewis base catalyzed enantioselective aldol addition of acetaldehyde-derived silyl enol ether to aldehydes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
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Tris(trimethylsilyl)silyl-governed aldehyde cross-aldol cascade reaction
1 reference
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https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
based on heuristic
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Proline-catalyzed mannich reaction of aldehydes with N-boc-imines
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
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Non-haemolytic beta-amino-acid oligomers
1 reference
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reference URL
https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
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Synthesis of β-Hexa- and β-Heptapeptides Containing Novel β2,3-Amino Acids with Two Serine or Two Cysteine Side Chains - CD- and NMR-Spectroscopic Evidence for 314-Helical Secondary Structures in Water
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
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Highly diastereoselective and enantioselective preparation of homoallylic amines: application for the synthesis of beta-amino acids and gamma-lactams
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Practical synthesis of enantiomerically pure beta2-amino acids via proline-catalyzed diastereoselective aminomethylation of aldehydes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oxazinanones as chiral auxiliaries: synthesis and evaluation in enolate alkylations and aldol reactions.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06740
retrieved
7 January 2021
based on heuristic
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The Mannich reaction of malonates with simple imines catalyzed by bifunctional cinchona alkaloids: enantioselective synthesis of beta-amino acids
1 reference
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https://api.crossref.org/works/10.1038%2FNATURE06740
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7 January 2021
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Identifiers
DOI
10.1038/NATURE06740
1 reference
stated in
Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
Dimensions Publication ID
1051882156
0 references
PubMed ID
18288105
1 reference
stated in
Europe PubMed Central
PubMed ID
18288105
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288105%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
ResearchGate publication ID
5564231
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