Access the full text.
Sign up today, get DeepDyve free for 14 days.
R. Pennington, R. Fisher (1981)
Dicyclohexylcarbodiimide modification of bovine heart mitochondrial transhydrogenase.The Journal of biological chemistry, 256 17
I. Ali, I. Al-Masoudi, B. Saeed, N. Al-Masoudi, P. Colla (2005)
Amino acid derivatives, part 2: Synthesis, antiviral, and antitumor activity of simple protected amino acids functionalized at N‐terminus with naphthalene side chainHeteroatom Chemistry, 16
E. El-Tamany, M. EL-Fattah, I. Ibrahim, E. Salem (1998)
Synthesis and Antimicrobial Activity of Some 1,2,4‐Triazoles.ChemInform, 29
J. Davies, A. Mohammed (1981)
Assessment of racemisation in N-alkylated amino-acid derivatives during peptide coupling in a model dipeptide systemJournal of The Chemical Society-perkin Transactions 1, 13
N. Al-Masoudi, I. Al-Masoudi, I. Ali, B. Saeed, P. Colla (2005)
Amino acid derivatives, part 3: New peptide and glycopeptide derivatives conjugated naphthalene. Synthesis, antitumor, anti‐HIV, and BVDV evaluationHeteroatom Chemistry, 16
D. Dogruer, S. Unlü, E. Yeşilada, M. Şahin (1997)
N-(2-pyridinyl)-2-[2(3H)-benzazolone-3-yl]acetamides: synthesis, antinociceptive and anti-inflammatory activity.Farmaco, 52 12
K. Waisser, J. Vanžura, A. Hrabálek, J. Vinšová, Š. Grešák, J. Hruška, Ž. Odlerová (1991)
Antimycobacterial derivatives of tetrazoleCollection of Czechoslovak Chemical Communications, 56
Walid Fathalla, M. Čajan, P. Pazdera (2000)
Regioselectivity of Electrophilic Attack on 4-Methyl-1-thioxo- 1,2,4,5-tetrahydro[1,2,4]triazolo[4,3-a]quinazolin-5-one. Part 1: Reactions at the Sulfur AtomMolecules : A Journal of Synthetic Chemistry and Natural Product Chemistry, 6
C. Lipinski (1986)
Chapter 27. Bioisosterism in Drug DesignAnnual Reports in Medicinal Chemistry, 21
G. Sahin, E. Palaska, M. Ekizoğlu, M. Ozalp (2002)
Synthesis and antimicrobial activity of some 1,3,4-oxadiazole derivatives.Farmaco, 57 7
Y. Goldgur, R. Craigie, G. Cohen, T. Fujiwara, T. Yoshinaga, T. Fujishita, H. Sugimoto, T. Endo, H. Murai, David Davies (1999)
Structure of the HIV-1 integrase catalytic domain complexed with an inhibitor: a platform for antiviral drug design.Proceedings of the National Academy of Sciences of the United States of America, 96 23
W. König, R. Geiger (1970)
Eine neue Methode zur Synthese von Peptiden: Aktivierung der Carboxylgruppe mit Dicyclohexylcarbodiimid unter Zusatz von 1‐Hydroxy‐benzotriazolenChemische Berichte, 103
R. Butler (1996)
4.17 – Tetrazoles, 4
C. Thornber (1979)
Isosterism and molecular modification in drug designChemical Society Reviews, 8
J. Adamec, K. Waisser, J. Kuneš, J. Kaustová (2005)
A Note on the Antitubercular Activities of 1‐Aryl‐5‐benzylsulfanyltetrazolesArchiv der Pharmazie, 338
R. Herr (2002)
5-Substituted-1H-tetrazoles as carboxylic acid isosteres: medicinal chemistry and synthetic methods.Bioorganic & medicinal chemistry, 10 11
Keita Noda, Y. Saad, A. Kinoshita, Thomas Boyle, R. Graham, A. Husain, S. Karnik (1995)
Tetrazole and Carboxylate Groups of Angiotensin Receptor Antagonists Bind to the Same Subsite by Different Mechanisms (*)The Journal of Biological Chemistry, 270
A new and convenient synthesis of a variety of N‐ and S‐substituted tetrazoles has been developed via azide and Mannich reaction methods. Compounds were characterized by elemental analysis, MALDI MS, and 1H NMR data. © 2007 Wiley Periodicals, Inc. Heteroatom Chem 18:637–643, 2007; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20353
Heteroatom Chemistry – Wiley
Published: Jan 1, 2007
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.