Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Siegfried N, Lodwig"'
Autor:
Siegfried N. Lodwig, Ernesto Juarez, David R. Glass, Marc A. Alvarez, Rodolfo A. Martinez, Erick Gabriel Ortiz, Clifford J. Unkefer
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 56:31-35
We have developed large-scale efficient procedures for the conversion of commercially available [(13) C]- or [(2) H3 ,(13) C]methanol and (13) CO2 or (13) C-labeled bromoacetic acid to 2-(phenylthio)[1,2-(13) C2 ]-, [1-(13) C]-, and [2-(13) C]acetic
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 55:211-222
13C labeled (>M + 4) metabolites of nitrogen and sulfur-based chemical warfare agent metabolites were prepared from readily available and 13C labeled commercial starting materials. The new chemical routes are efficient in the number of chemical steps
Autor:
Yoshio Takeuchi, Tomoya Fujiwara, Taiki Murai, Tamiko Takahashi, Kenji Omata, Clifford J. Unkefer, Kuninobu Kabuto, Masaru Segawa, Siegfried N. Lodwig, Hidehito Fujisawa
Publikováno v:
Tetrahedron: Asymmetry. 19:847-856
Applications of the CFTA method, a new and reliable procedure for the determination of the absolute configuration of chiral primary amines, are described in detail. In addition to the very high reactivity of CFTA chloride, the stable anti-periplanar
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 41:983-991
We have developed a stereoselective route to the synthesis of stable isotope-labeled L-proline. Alkylation of (2R)-N-(N'-[bis(methylthio)methylidene}-glycyl)bornane-10,2-sultam with 3-chloro-iodopropane yielded (2R)-N-{(2'S)-2'-([Bis(methylthio)methy
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 38:239-248
Using 1-chloro-1-[ 15 N]nitrosocyclohexane, we have prepared five L-[α- 15 N]amino acids. The stereoselective electophillic hydroxyamination of (S)-acylbornane-10,2-sultams, followed by Zn°/H + reduction, and alkaline cleavage of the chiral auxilia
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 38:161-167
We have prepared 1-chloro-1-[ 15 N]nitrosocyclohexane, an electrophillic aminating reagent useful for the stereoselective synthesis of α-[ 15 N]amino acids. Treatment of potassium [ 15 N]nitrate with Pb° gave potassium [ 15 N]nitrite, which was con
Autor:
Rodolfo A, Martinez, David R, Glass, Erick G, Ortiz, Marc A, Alvarez, Ernesto, Juarez, Siegfried N, Lodwig, Clifford J, Unkefer
Publikováno v:
Journal of labelled compoundsradiopharmaceuticals. 56(2)
We have developed large-scale efficient procedures for the conversion of commercially available [(13) C]- or [(2) H3 ,(13) C]methanol and (13) CO2 or (13) C-labeled bromoacetic acid to 2-(phenylthio)[1,2-(13) C2 ]-, [1-(13) C]-, and [2-(13) C]acetic
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 31:95-102
We have developed a stereoselective route to isotopically labeled L-aspartic acid using L-serine as a chiral precursor. Labeled serine, prepared biosynthetically was N-protected by conversion to the N-t-Boc derivative. (N-t-Boc)-[3−13C]Serine is cy
Autor:
Louis A. Silks, Deborah S. Ehler, Clifford J. Unkefer, Rowena Gibson, Siegfried N. Lodwig, John L. Hanners
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 29:1247-1256
We have developed a stereospecific chemomicrobiological synthesis of labeled tryptophan. L-[3-13C]Serine, [1-15N]- and [2-13C]indole were used as precursors for the synthesis of L-[β-13C]-, L-[1′-15N]-, and L-[2′-13C]tryptophan, respectively. Th
Autor:
Clifford J. Unkefer, Robert E. London, William A. Beard, Siegfried N. Lodwig, Rajendra Prasad, Samuel H. Wilson, Guanghua Gao
Determination of the protonation state of titratable protein residues is of critical importance for the interpretation of active site chemistry, as well as for understanding the role of electrostatic interactions in protein folding and stability. How
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc98b06b6a49319eb0efa5e46c33101b
https://europepmc.org/articles/PMC2846763/
https://europepmc.org/articles/PMC2846763/