Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,237,304 papers from all fields of science
Search
Sign In
Create Free Account
Glyoxylate/Creatinine:SRto:Pt:Urine:Qn
Known as:
Glyoxylat/Kreatinin:SKRto:Pkt:Urin:Qn
, Glyoxylate/creat Ur-sRto
, glioxalato/creatinina:relación de concentración de la sustancia:punto en el tiempo:orina:cuantitativo
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
5 relations
Chemical procedure
Creatinine
Glyoxylates
Substance Ratio
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Catalytic Asymmetric Mannich Reaction with N-Carbamoyl Imine Surrogates of Formaldehyde and Glyoxylate.
Yang'en You
,
Long Zhang
,
Linfeng Cui
,
X. Mi
,
S. Luo
Angewandte Chemie
2017
Corpus ID: 29983845
N,O-acetals (NOAcs) were developed as bench stable surrogates for N-carbamoyl, (Boc, Cbz and Fmoc) formaldehyde and glyoxylate…
Expand
2016
2016
Catalytic Asymmetric Prins Bicyclization for the endo-Selective Formation of 2,6-dioxabicyclo[2.2.2]octanes.
Jie Liu
,
Lijun Zhou
,
+5 authors
A. Goeke
Chemistry
2016
Corpus ID: 29499904
A new Lewis acid-catalyzed endo-selective Prins bicyclization of γ,δ-unsaturated aldehydes or ketones with a broad range of…
Expand
2013
2013
Asymmetric synthesis and catalytic activity of 3-methyl-β-proline in enantioselective anti-Mannich-type reactions.
K. Nagata
,
Yasushi Kuga
,
+4 authors
T. Itoh*
Journal of Organic Chemistry
2013
Corpus ID: 11578076
Enantiomerically pure 3-methyl-β-proline was synthesized using an asymmetric phase-transfer-catalyzed alkylation of a…
Expand
2008
2008
3-trifluoromethanesulfonamido-pyrrolidine: a general organocatalyst for anti-selective mannich reactions.
M. Pouliquen
,
J. Blanchet
,
M. Lasne
,
J. Rouden
Organic Letters
2008
Corpus ID: 46457110
Mannich-type reactions of a glyoxylate imine with carbonyl compounds catalyzed by 3-trifluoromethanesulfonamidopyrrolidine…
Expand
2006
2006
Regiospecific one-pot synthesis of pyrimido[4,5-d]pyrimidine derivatives in the solid state under microwave irradiations.
D. Prajapati
,
Mukut Gohain
,
A. Thakur
Bioorganic & Medicinal Chemistry Letters
2006
Corpus ID: 2018663
2004
2004
A new class of substituted aryl bis(oxazoline) ligands for highly enantioselective copper-catalyzed asymmetric aldol addition of dienolsilane to pyruvate and glyoxylate esters.
J. Le
,
B. Pagenkopf
Organic Letters
2004
Corpus ID: 31480735
[reaction: see text] A new class of bis(oxazoline) ligands are introduced that feature o-alkoxyaryl substituents and provide the…
Expand
Highly Cited
2000
Highly Cited
2000
C2-Symmetric Copper(II) Complexes as Chiral Lewis Acids. Catalytic Enantioselective Carbonyl−Ene Reactions with Glyoxylate and Pyruvate Esters
D. A. Evans
,
Steven W. Tregay
,
C. Burgey
,
Andrea Paras
,
T. Vojkovský
2000
Corpus ID: 42865295
The C2-symmetric complexes [Cu(S,S)-tert-butylbis(oxazolinyl)](SbF6)2 (2a), its bis(aquo) counterpart [Cu(S,S)-tert-butylbis…
Expand
Highly Cited
2000
Highly Cited
2000
Catalytic enantioselective aza-Diels-alder reactions of imines--an approach to optically active nonproteinogenic alpha-amino acids
Yao
,
Saaby
,
Hazell
,
Jørgensen
Chemistry
2000
Corpus ID: 28306279
A catalytic enantioselective aza-Diels-Alder reaction of imines has been developed. The reaction of N-tosyl alpha-imino ester…
Expand
Highly Cited
1998
Highly Cited
1998
C2-SYMMETRIC COPPER(II) COMPLEXES AS CHIRAL LEWIS ACIDS. ENANTIOSELECTIVE CATALYSIS OF THE GLYOXYLATE-ENE REACTION
D. A. Evans
,
C. Burgey
,
Nick A. Paras
,
T. Vojkovský
,
Steven W. Tregay
1998
Corpus ID: 98284507
The development of enantioselective Lewis acid catalyzed carbonyl addition reactions of π-nucleophiles such as enolsilanes and…
Expand
1996
1996
ASYMMETRIC HETERO DIELS-ALDER REACTIONS OF DANISHEFSKY'S DIENE AND GLYOXYLATE ESTERS CATALYZED BY CHIRAL BISOXAZOLINE DERIVED CATALYSTS.
Arun K. Ghosh
,
P. Mathivanan
,
J. Cappiello
,
K. Krishnan
Tetrahedron: asymmetry
1996
Corpus ID: 53234903
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE