Статті в журналах з теми "Hydroxyethylene isosters"
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JONES, D. M., B. NILSSON, and M. SZELKE. "ChemInform Abstract: A Short Stereocontrolled Synthesis of Hydroxyethylene Dipeptide Isosters." ChemInform 24, no. 39 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199339146.
Повний текст джерелаD'ANIELLO, F., S. GEHANNE, and M. TADDEI. "ChemInform Abstract: A Convenient Approach to Hydroxyethylene Dipeptide Isosters Using Allylsilane Chemistry." ChemInform 24, no. 6 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199306274.
Повний текст джерелаGHOSH, A. K., S. P. MCKEE, and W. J. THOMPSON. "ChemInform Abstract: An Efficient Synthesis of Hydroxyethylene Dipeptide Isosters: The Core Unit of Potent HIV-1 Protease Inhibitors." ChemInform 23, no. 13 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199213295.
Повний текст джерелаROSENBERG, S. H., S. A. BOYD, and R. A. MANTEI. "ChemInform Abstract: A Stereoselective Synthesis of Hydroxyethylene and erythro- Dihydroxyethylene Dipeptide Isosters: A Facial Selective anti-Aldol Reaction." ChemInform 23, no. 28 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199228054.
Повний текст джерелаDanielmeier, Karsten, Kerstin Schierle та Eberhard Steckhan. "A New Chiral, Cationicβ-Amino Alcohol Equivalent: A Variable Approach to Enantiomerically Pure Building Blocks for Hydroxyethylene Isosters". Angewandte Chemie International Edition in English 35, № 19 (18 жовтня 1996): 2247–48. http://dx.doi.org/10.1002/anie.199622471.
Повний текст джерелаLindgren, Cecilia, Ida E. Andersson, Lotta Berg, Doreen Dobritzsch, Changrong Ge, Sabrina Haag, Urszula Uciechowska, Rikard Holmdahl, Jan Kihlberg, and Anna Linusson. "Hydroxyethylene isosteres introduced in type II collagen fragments substantially alter the structure and dynamics of class II MHC Aq/glycopeptide complexes." Organic & Biomolecular Chemistry 13, no. 22 (2015): 6203–16. http://dx.doi.org/10.1039/c5ob00395d.
Повний текст джерелаMarinier, Aime, Mihaly V. Toth, Kathryn Houseman, Richard Mueller, and Garland R. Marshall. "HIV-1 protease inhibitors: Ketomethylene isosteres with unusually high affinity compared with hydroxyethylene isostere analogs." Bioorganic & Medicinal Chemistry 2, no. 9 (September 1994): 919–25. http://dx.doi.org/10.1016/s0968-0896(00)82041-6.
Повний текст джерелаBoyd, Steven A., Robert A. Mantei, Chi Nung Hsiao, and William R. Baker. "Stereoselective syntheses of hydroxyethylene dipeptide isosteres." Journal of Organic Chemistry 56, no. 1 (January 1991): 438–42. http://dx.doi.org/10.1021/jo00001a083.
Повний текст джерелаKONIECZNY, M. T., P. H. TOMA, and M. CUSHMAN. "ChemInform Abstract: Synthesis of Hydroxyethylene Isosters of the Transition State of the HIV Protease-Catalyzed Phe-Pro Hydrolysis: Reaction of 2-((Boc)amino)- 1-(2′-oxocyclopentyl)-3-phenylpropanols with Diethyl Phosphorocyanidate and Lithium Cyanide Fo." ChemInform 24, no. 51 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199351192.
Повний текст джерелаDiederich, Ann M., and David M. Ryckman. "Stereoselective synthesis of a hydroxyethylene dipeptide isostere." Tetrahedron Letters 34, no. 39 (September 1993): 6169–72. http://dx.doi.org/10.1016/s0040-4039(00)73701-4.
Повний текст джерелаChakraborty, T. K., and K. K. Gangakhedkar. "Stereoselective Synthesis of Hydroxyethylene Dipeptide Isostere from Sugar." Synthetic Communications 26, no. 11 (June 1996): 2045–56. http://dx.doi.org/10.1080/00397919608003563.
Повний текст джерелаTao, Junhua, and Robert V. Hoffman. "A Stereocontrolled, Convergent Synthesis of Hydroxyethylene Dipeptide Isosteres." Journal of Organic Chemistry 62, no. 18 (September 1997): 6240–44. http://dx.doi.org/10.1021/jo970579s.
Повний текст джерелаPégorier, Laurent, and Marc Larchevêque. "A general stereocontrolled synthesis of hydroxyethylene dipeptide isosteres." Tetrahedron Letters 36, no. 16 (April 1995): 2753–56. http://dx.doi.org/10.1016/0040-4039(95)00357-i.
Повний текст джерелаKempf, Dale J. "Dipeptide analogs. Versatile synthesis of the hydroxyethylene isostere." Journal of Organic Chemistry 51, no. 21 (October 1986): 3921–26. http://dx.doi.org/10.1021/jo00371a001.
Повний текст джерелаWuts, Peter G. M., Allen R. Ritter, and Lynn E. Pruitt. "Synthesis of the hydroxyethylene isostere of Leu-Val." Journal of Organic Chemistry 57, no. 25 (December 1992): 6696–700. http://dx.doi.org/10.1021/jo00051a005.
Повний текст джерелаJones, D. Michael, Bo Nilsson, and Michael Szelke. "A short stereocontrolled synthesis of hydroxyethylene dipeptide isosteres." Journal of Organic Chemistry 58, no. 8 (April 1993): 2286–90. http://dx.doi.org/10.1021/jo00060a052.
Повний текст джерелаBOYD, S. A., R. A. MANTEI, C. N. HSIAO, and W. R. BAKER. "ChemInform Abstract: Stereoselective Syntheses of Hydroxyethylene Dipeptide Isosteres." ChemInform 22, no. 21 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199121267.
Повний текст джерелаHerold, Peter, Rudolph Duthaler, Grety Rihs, and Christof Angst. "A versatile and stereocontrolled synthesis of hydroxyethylene dipeptide isosteres." Journal of Organic Chemistry 54, no. 5 (March 1989): 1178–85. http://dx.doi.org/10.1021/jo00266a034.
Повний текст джерелаPeyrat, Jean-François, Christophe Chaboche, Bruno Figadère, and André Cavé. "A formal stereoselective synthesis of a hydroxyethylene dipeptide isostere." Tetrahedron Letters 36, no. 16 (April 1995): 2757–60. http://dx.doi.org/10.1016/0040-4039(95)00358-j.
Повний текст джерелаAoyagi, Yutaka, and Robert M. Williams. "General asymmetric synthesis of hydroxymethylene and hydroxyethylene peptide isosteres." Tetrahedron 54, no. 35 (August 1998): 10419–33. http://dx.doi.org/10.1016/s0040-4020(98)00495-5.
Повний текст джерелаDIEDERICH, A. M., and D. M. RYCKMAN. "ChemInform Abstract: Stereoselective Synthesis of a Hydroxyethylene Dipeptide Isostere." ChemInform 25, no. 12 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199412271.
Повний текст джерелаErdal, Erik P., Pavel Martásek, Linda J. Roman, and Richard B. Silverman. "Hydroxyethylene isosteres of selective neuronal nitric oxide synthase inhibitors." Bioorganic & Medicinal Chemistry 15, no. 18 (September 2007): 6096–108. http://dx.doi.org/10.1016/j.bmc.2007.06.038.
Повний текст джерелаLitera, Jaroslav, Miloš Buděšínský, Ján Urban, and Milan Souček. "Peptide Inhibitors of Aspartic Proteinases with Hydroxyethylene Isostere Replacement of Peptide Bond. I. Preparation of Four Diastereoisomeric (2R or 2S,4R or 4S,5S)-2-Benzyl-5-[(tert-butoxycarbonyl)amino]-4-hydroxy-6-phenylhexanoic Acids." Collection of Czechoslovak Chemical Communications 63, no. 2 (1998): 231–44. http://dx.doi.org/10.1135/cccc19980231.
Повний текст джерелаDragovich, Peter S., Thomas J. Prins, and Ru Zhou. "Formal, Stereoselective Synthesis of Hydroxyethylene Dipeptide Isosteres Utilizing Pseudoephedrine Amides." Journal of Organic Chemistry 62, no. 22 (October 1997): 7872–76. http://dx.doi.org/10.1021/jo9707951.
Повний текст джерелаD'Aniello, Fabiana, Sylvie Géhanne, and Maurizio Taddei. "A convenient approach to hydroxyethylene dipeptide isosteres using allylsilane chemistry." Tetrahedron Letters 33, no. 38 (September 1992): 5621–24. http://dx.doi.org/10.1016/s0040-4039(00)61163-2.
Повний текст джерелаYang, Xiaoming, Xiaomin Zou, Yiqiu Fu, Ke Mou, Gang Fu, Chao Ma та Ping Xu. "Synthesis of β‐Secretase Inhibitors Containing a Hydroxyethylene Dipeptide Isostere". Synthetic Communications 37, № 1 (1 січня 2007): 9–24. http://dx.doi.org/10.1080/00397910600977509.
Повний текст джерелаNishi, Takahide, Mitsuru Kataoka, and Yasuhiro Morisawa. "Diastereoselective Synthesis of the Hydroxyethylene Dipeptide Isostere of Leu–Val." Chemistry Letters 18, no. 11 (November 1989): 1993–96. http://dx.doi.org/10.1246/cl.1989.1993.
Повний текст джерелаPEGORIER, L., and M. LARCHEVEQUE. "ChemInform Abstract: A General Stereocontrolled Synthesis of Hydroxyethylene Dipeptide Isosteres." ChemInform 26, no. 32 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199532205.
Повний текст джерелаCHAKRABORTY, T. K., and K. K. GANGAKHEDKAR. "ChemInform Abstract: Stereoselective Synthesis of Hydroxyethylene Dipeptide Isostere from Sugar." ChemInform 27, no. 36 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199636207.
Повний текст джерелаTAO, J., and R. V. HOFFMAN. "ChemInform Abstract: A Stereocontrolled, Convergent Synthesis of Hydroxyethylene Dipeptide Isosteres." ChemInform 29, no. 3 (June 24, 2010): no. http://dx.doi.org/10.1002/chin.199803209.
Повний текст джерелаShin, Hyunik, Kyu Woong Lee, Hyeong-wook Choi, Byung Han Lee, Bo Seung Choi, Jay Hyok Chang, Young Keun Kim, Jae Hoon Lee, Taeho Heo, and Do Hyun Nam. "A Stereodivergent Synthesis of Hydroxyethylene Dipeptide Isostere via Highly Diastereoselective Epoxidation." Synlett, no. 20 (2005): 3136–38. http://dx.doi.org/10.1055/s-2005-921907.
Повний текст джерелаStuk, Timothy L., Anthony R. Haight, David Scarpetti, Michael S. Allen, Jerome A. Menzia, Timothy A. Robbins, Shyamal I. Parekh, Denton C. Langridge, and Jien-Heh J. Tien. "An Efficient Stereocontrolled Strategy for the Synthesis of Hydroxyethylene Dipeptide Isosteres." Journal of Organic Chemistry 59, no. 15 (July 1994): 4040–41. http://dx.doi.org/10.1021/jo00094a006.
Повний текст джерелаAOYAGI, Y., and R. M. WILLIAMS. "ChemInform Abstract: General Asymmetric Synthesis of Hydroxymethylene and Hydroxyethylene Peptide Isosteres." ChemInform 29, no. 52 (June 18, 2010): no. http://dx.doi.org/10.1002/chin.199852094.
Повний текст джерелаPEYRAT, J. F., C. CHABOCHE, B. FIGADERE, and A. CAVE. "ChemInform Abstract: A Formal Stereoselective Synthesis of a Hydroxyethylene Dipeptide Isostere." ChemInform 26, no. 32 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199532206.
Повний текст джерелаNadin, Alan, Andrew P. Owens, José L. Castro, Timothy Harrison та Mark S. Shearman. "Synthesis and γ-secretase activity of APP substrate-based hydroxyethylene dipeptide isosteres". Bioorganic & Medicinal Chemistry Letters 13, № 1 (січень 2003): 37–41. http://dx.doi.org/10.1016/s0960-894x(02)00840-5.
Повний текст джерелаBrewer, Matthias, Clint A. James, and Daniel H. Rich. "Synthesis of a Tripeptide Derivative Containing the Gln-Arg Hydroxyethylene Dipeptide Isostere." Organic Letters 6, no. 25 (December 2004): 4779–82. http://dx.doi.org/10.1021/ol047880x.
Повний текст джерелаSakurai, Mitsuya, Fujio Saito, Yasuo Ohata, Yuichiro Yabe та Takahide Nishi. "An efficient synthesis of γ-lactones as precursors of hydroxyethylene dipeptide isostere". J. Chem. Soc., Chem. Commun., № 21 (1992): 1562–63. http://dx.doi.org/10.1039/c39920001562.
Повний текст джерелаBrewer, Matthias, and Daniel H. Rich. "Synthesis of a Tripeptide Derivative Containing the Phe-Arg Hydroxyethylene Dipeptide Isostere." Organic Letters 3, no. 6 (March 2001): 945–48. http://dx.doi.org/10.1021/ol015612i.
Повний текст джерелаWilliams, Robert M. "ChemInform Abstract: Asymmetric Syntheses of Unnatural Amino Acids and Hydroxyethylene Peptide Isosteres." ChemInform 31, no. 30 (June 7, 2010): no. http://dx.doi.org/10.1002/chin.200030268.
Повний текст джерелаBaker, William R., та John K. Pratt. "Dipeptide isosteres. 2. Synthesis of hydroxyethylene dipeptide isostere diastereomers from a common γ-lactone intermediate. Preparation of renin and HIV-1 protease inhibitor transition state mimics." Tetrahedron 49, № 39 (січень 1993): 8739–56. http://dx.doi.org/10.1016/s0040-4020(01)81896-2.
Повний текст джерелаSakurai, Mitsuya, Tadashi Hata та Yuichiro Yabe. "A new synthetic route for the γ-lactone precursors of hydroxyethylene dipeptide isosteres". Tetrahedron Letters 34, № 37 (вересень 1993): 5939–42. http://dx.doi.org/10.1016/s0040-4039(00)73819-6.
Повний текст джерелаRadunz, Hans-Eckart, Volker Eiermann, Günther Schneider, and Angelika Riethmüller. "A convenient approach to hydroxyethylene dipeptide isosteres as building blocks for enzyme inhibitors." Tetrahedron 47, no. 10-11 (March 1991): 1887–94. http://dx.doi.org/10.1016/s0040-4020(01)96101-0.
Повний текст джерелаSTUK, T. L., A. R. HAIGHT, D. SCARPETTI, M. S. ALLEN, J. A. MENZIA, T. A. ROBBINS, S. I. PAREKH, et al. "ChemInform Abstract: An Efficient Stereocontrolled Strategy for the Synthesis of Hydroxyethylene Dipeptide Isosteres." ChemInform 26, no. 4 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199504237.
Повний текст джерелаChakraborty, T. K., K. Azhar Hussain, and D. Thippeswamy. "A simple strategy for the synthesis of hydroxyethylene dipeptide isostere from D-glucose." Tetrahedron 51, no. 13 (March 1995): 3873–80. http://dx.doi.org/10.1016/0040-4020(95)00109-l.
Повний текст джерелаWångsell, Fredrik, Karin Gustafsson, Ingemar Kvarnström, Neera Borkakoti, Michael Edlund, Katarina Jansson, Jimmy Lindberg, Anders Hallberg, Åsa Rosenquist, and Bertil Samuelsson. "Synthesis of potent BACE-1 inhibitors incorporating a hydroxyethylene isostere as central core." European Journal of Medicinal Chemistry 45, no. 3 (March 2010): 870–82. http://dx.doi.org/10.1016/j.ejmech.2009.11.013.
Повний текст джерелаKIM, B. H., and H. J. AHN. "ChemInform Abstract: Efficient Synthesis of Hydroxyethylidene and (E)-Alkene Dipeptide Isosteres." ChemInform 28, no. 46 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199746204.
Повний текст джерелаChakraborty, T. K., and S. Dutta. "Synthesis of a New C2-Symmetric Molecule with Dimeric Hydroxyethylene Isosteric Moiety." Synthetic Communications 27, no. 23 (December 1997): 4163–72. http://dx.doi.org/10.1080/00397919708005464.
Повний текст джерелаLagu, Bharat R., and Dennis C. Liotta. "Diastereoselective synthesis of the key lactone intermediate for the preparation of hydroxyethylene dipeptide isosteres." Tetrahedron Letters 35, no. 4 (January 1994): 547–50. http://dx.doi.org/10.1016/s0040-4039(00)75834-5.
Повний текст джерелаThompson, Wayne J., Richard G. Ball, Paul L. Darke, Joan A. Zugay, and J. E. Thies. "Stereoselective synthesis of the hydroxyethylene isostere of the HIV protease (Tyr-Pro) cleavage site." Tetrahedron Letters 33, no. 21 (May 1992): 2957–60. http://dx.doi.org/10.1016/s0040-4039(00)79571-2.
Повний текст джерелаHolladay, Mark W., Francesco G. Salituro, and Daniel H. Rich. "Synthetic and enzyme inhibition studies of pepstatin analogs containing hydroxyethylene and ketomethylene dipeptide isosteres." Journal of Medicinal Chemistry 30, no. 2 (February 1987): 374–83. http://dx.doi.org/10.1021/jm00385a020.
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