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162 Gu, H M; Lu, B F; Qu, Z Q Antimalarial activities of 25 derivatives of artemisinin against chloroquine-resistant Plasmodium berghei Acta Pharmacol Sin, 1980, 1: 48 50 163 Yu, P L; Chen, Y X; Li, Y; Ji, R Y Studies on analogs of artemisinin IV Synthesis of derivatives of qinghaosu containing halogen, nitrogen and sulfur heteroatoms Chin Pharmaceu Bull, 1980, 15: 44; Acta Pharmaceu Sin, 1985, 20: 357 365 164 Pu, Y M; Torok, D S; Ziffer, H; Pan, X-Q; Meshnick, S R Synthesis and antimalarial activities of several uorinated artemisinin derivatives J Med Chem, 1995, 38: 4120 4124 165 Abouabdellah, A; Begue, J-P; Bonnet-Delpon, D; Gantier, J C; Truong Thi Thanh, N; Truong, D T Synthesis and in vivo antimalarial activity of 12 a-tri uoromethylhydroartemisinin Bioorg Med Chem.

Lett, 1996, 6: 2717 2720 166 Nga, T T T; Menage, C; Begue, J-P; Bonnet-Delpon, D; Gantier, J-C; Pradines, B; Doury, J-C; Thac, T Synthesis and antimalarial activities of uoroalkyl derivatives of dihydroartemisinin J Med Chem, 1998, 41: 4101 4108 167 Magueur, G; Crousse, B; Charneau, S; Grellier, P; Begue, J-P; Bonnet-Delpon, D Fluoroartemisinin: Tri uoromethyl analogues of artemether and artesunate J Med Chem, 2004, 47: 2694 2699 168 Venugopalan, B; Karnik, P J; Bapat, C P; Chatterjee, D K; Iyer, N; Lepcha, D Antimalarial activity of new ethers and thioethers of dihydroartemisinin Eur J Med Chem, 1995, 30: 697 706 169 Haynes, R K; Chan, H W; Cheung, M K; Lam, W L; Soo, M K; Tsang, H W.

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; Voerste, A; Williams, I D C-10 Ester and ether derivatives of dihydroartemisinin-10a artesunate, preparation of authentic 10-b artesunate, and of other ester and ether derivatives bearing potential aromatic intercalating groups at C-10 Eur J Org Chem, 2002, 1: 113 132 170 Liang, J; Li, Y Synthesis of the aryl ether derivatives of artemisinin Chinese J Med Chem, 1996, 6: 22 25 171 O Neill, P M; Miller, A; Bishop, L P D; Hindley, S; Maggs, J L; Ward, S A; Roberts, S M; Scheinmann, F; Stachulski, A V; Posner, G H; Park, B K Synthesis, antimalarial activity, biomimetic iron(II) chemistry, and in-vivo metabolism of novel, potent C-10-phenoxy derivatives of dihydroartemisinin J Med Chem, 2001, 44: 58 68 172 Yang, Y H; Li, Y; Shi, Y L; Yang, J D.

This book focuses on open source software. That is not to say that open source software represents the only affordable J2EE solution for the many types of people or organizations that may need a J2EE platform. For example, Sun provides the J2EE reference environment for free. Although it cannot be used to deploy an application, the J2EE reference environment is suitable for learning purposes. The products evaluated and discussed in this book are all open source. All discussion is based on the latest stable version of each product at the time of writing. For some products this may mean that the product is a beta release; however, our focus is on stable releases. Alpha and unstable products that may have merit are discussed more briefly so that the reader knows to monitor the project for potential future application.

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; Wu, B A Artemisinin derivatives with 12aniline substitution: Synthesis and antimalarial activity Bioorg Med Chem Lett, 1995, 5: 1791 1794 173 Li, Y; Liao, X B CN Patent: ZL 99,124,012 174 Jung, M; Bustos, D A; El-Sohly, H N; McChesney, J D A concise and stereoselective synthesis of ( )-12-n-butyldeoxoartemisinin Synlett, 1990, 743 744 175 Jung, M; Yu, D Y; Bustos, D; El-Sohly, H N; McChesney, J D A concise synthesis of 12(30 -hydroxy-n-propyl)-deoxoartemisinin Bioorg Med Chem Lett, 1991, 1: 741 744 176 Haynes, R K; Vonwiller, S C Effecient preparation of novel qinghaosu(artemisinin) derivatives: Conversion of qinghaosu (artemisinic) acid into deoxoqinghaosu derivatives and 5-carba-4-deoxoartesunic acid Synlett, 1992, 481 483 177 Pu, Y M; Ziffer, H Synthesis and antimalarial activities of 12b-allyldeoxoartemisinin and its derivatives J Med Chem, 1995, 38: 613 616 178.

Ma, J Y; Katz, E; Ziffer, H A new synthetic route to 10-beta-alkyl deoxoartemisinins Tetrahedron Lett, 1999, 40: 8543 8545..

1.2 kbit/s 2.4 kbit/s 9.6 kbit/s FLEX 64 kbit/s MUX (n = 1)

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Freston says, Well, Sancho, although you (fortunately, even luckily) got the same output to the screen that I did, you didn t really get the same result. When I cat d my errfile, I found it to be empty. So I m confident that I was able to examine all directories. Is your errfile empty Sancho checks and tells him, No way! My errfile is full of errors! Many directories didn t allow me entry at all! The lesson here is to be careful with commands like this one. If the command does not appear to provide the expected output, or even if it does, it might still have created errors. But you will not know about the errors unless you check the errfile file. An ordinary user (as opposed to a superuser or a root user) is likely to encounter more errors in these situations due to a lack of permissions on directories or files.

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