Authors:
Shafiee, A
Tsipouras, A
Bouffard, A
Onishi, JC
Guan, ZQ
Motamedi, H
Citation: A. Shafiee et al., Enzymatic deglycosylation of enfumafungin, a triterpene glycoside natural product, and its chemically synthesized analogues, J MOL CAT B, 16(1), 2001, pp. 27-32
Authors:
Shafiee, A
Harris, G
Motamedi, H
Rosenbach, M
Chen, T
Zink, D
Heimbuch, B
Citation: A. Shafiee et al., Microbial hydroxylation of rustmicin (galbonolide A) and galbonolide B, two antifungal products produced by Micromonospora sp., J MOL CAT B, 11(4-6), 2001, pp. 237-242
Authors:
Jalilian, AR
Seyfi, P
Afarideh, H
Shafiee, A
Citation: Ar. Jalilian et al., Synthesis of a [F-18]labeled chelidonine derivative as a possible antitumor agent, APPL RAD IS, 54(3), 2001, pp. 407-411
Citation: S. Emami et A. Shafiee, Stereoselective syntheses of (E)- and (Z)-2,3-dihydro-3-(1,2,4-triazolyl)-4H-1-benzopyran-4-one oxime ethers, HETEROCYCLE, 55(11), 2001, pp. 2059-2074
Authors:
Jalilian, AR
Bineshmarvasti, M
Rafii, H
Afarideh, H
Shafiee, A
Citation: Ar. Jalilian et al., No-carrier-added, F-18-labelling of a cholesterol derivative, used in detection of adrenal malignancies, J LABEL C R, 44(11), 2001, pp. 747-755
Authors:
Singh, SB
Jayasuriya, H
Salituro, GM
Zink, DL
Shafiee, A
Heimbuch, B
Silverman, KC
Lingham, RB
Genilloud, O
Teran, A
Vilella, D
Felock, P
Hazuda, D
Citation: Sb. Singh et al., The complestatins as HIV-1 integrase inhibitors. Efficient isolation, structure elucidation, and inhibitory activities of isocomplestatin, chloropeptin I, new complestatins, A and B, and acid-hydrolysis products of chloropeptin I, J NAT PROD, 64(7), 2001, pp. 874-882
Citation: A. Foroumadi et al., Antituberculosis agents, I: Synthesis and antituberculosis activity of 2-aryl-1,3,4-thiadiazole derivatives, PHARMAZIE, 56(8), 2001, pp. 610-612
Authors:
Jalilian, AR
Afarideh, H
Najafi, R
Shafiee, A
Bineshmarvasti, M
Citation: Ar. Jalilian et al., A new method for one-step, no-carrier-added synthesis of cholesteryl 4-[F-18]-fluorobenzoate ([F-18]-CFB), a radiotracer used in detection of adrenalmalignancies, J PHARM P S, 3(1), 2000, pp. 118-124
Authors:
Jalilian, AR
Sattari, S
Bineshmarvasti, M
Shafiee, A
Daneshtalab, M
Citation: Ar. Jalilian et al., Synthesis and in vitro antifungal and cytotoxicity evaluation of thiazolo-4H-1,2,4-triazoles and 1,2,3-thiadiazolo-4H-1,2,4-triazoles, ARCH PHARM, 333(10), 2000, pp. 347-354
Authors:
Jalilian, AR
Tabatabai, SA
Shafiee, A
Afarideh, H
Najafi, R
Bineshmarvasti, M
Citation: Ar. Jalilian et al., One-step, no-carrier-added, synthesis of a F-18-labelled benzodiazepine receptor ligand, J LABEL C R, 43(6), 2000, pp. 545-555
Citation: A. Shafiee et al., Selenium heterocycles XLIV. Syntheses of 8,9-dihydro-1,2,3-thiadiazolo[4,5-a]-4,7-dihydroxynaphthalene and 1,2,3-selenadiazolo[4,5-a]-4,7-dimethoxynaphthalene, J HETERO CH, 37(5), 2000, pp. 1325-1327
Citation: A. Shafiee et al., Syntheses of 2-alkylthio-1-[4-(N-alpha-ethoxycarbonylbenzyl)-aminobenzyl]-5-hydroxymethylimidazoles, J HETERO CH, 37(4), 2000, pp. 1015-1018
Authors:
Singh, SB
Zink, D
Polishook, J
Valentino, D
Shafiee, A
Silverman, K
Felock, P
Teran, A
Vilella, D
Hazuda, DJ
Lingham, RB
Citation: Sb. Singh et al., Structure and absolute stereochemistry of HIV-1 integrase inhibitor integric acid. A novel eremophilane sesquiterpenoid produced by a Xylaria sp., TETRAHEDR L, 40(50), 1999, pp. 8775-8779
Citation: A. Shafiee et al., Selenium heterocycles. XLIII [1]. Syntheses of 3,5-diaryl-1,2,4-thiadiazoles and 3,5-diaryl-1,2,4-selenadiazoles, J HETERO CH, 36(4), 1999, pp. 901-903
Authors:
Chen, TS
Li, XH
Petuch, B
Shafiee, A
So, L
Citation: Ts. Chen et al., Structural modification of the immunosuppressants FK-506 and ascomycin using a biological approach, CHIMIA, 53(12), 1999, pp. 596-600
Authors:
Tabatabai, SA
Zarrindast, MR
Lashkari, SB
Shafiee, A
Citation: Sa. Tabatabai et al., Synthesis, conformational analysis and antinociceptive activity of 1-[N-methyl-(2-phenylethyl)amino]methyl-1,2,3,4-tetrahydroisoquinoline derivatives, ARZNEI-FOR, 49(12), 1999, pp. 1001-1005
Citation: A. Foroumadi et al., Synthesis and in vitro antifungal activity of 2-aryl-5-phenylsulfonyl-1,3,4-thiadiazole derivatives, ARZNEI-FOR, 49(12), 1999, pp. 1035-1038