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##ates chloro solv ##ative includ ##stit ##here mod ##ance ##ond bet there 18 ##onyl method fluor cr ##nt amino tet ##sol 40 described ##vi rec press em sil comb fl ##ography ##ular remo sal purified ##queous ##idine ##ose aqueous spec cal ##we sulf pos pol rel filtered ##vention cycl ##ors 17 about chromatography eff dm ##rim ##end dimethyl dat ##ased contain ##ection ##ym no ##amine until more pressure ##bod ##ating oil prote 24 ##ob na addition ##ient these 60 solvent hex ##own bo ##olog ##ica sign reduced ##io gel ##atur ##ween between prop ##ind vac ##ist prepared nit ##ari man cor ##res ##als dissol cons step formul chloride ##de extracted also differ layer ca have tetra ##oxyl resp ##hes ##ld ##row colum reg ##str analysis column ser fur protein silica other two activ ##ichlor out ##amide data vacu ##apor bl fig ##ame 35 ##oprop butyl brom str ##ction ##of ##ients ##osph dissolved ##ome ##ise evapor ##ort time sim ##ong ##ear where comple ref 22 prov pot dichlor perform pi ##sp methoxy present ##ression aff mon accord ##gg carbon bi ##ber resulting methanol ##ok substit partic gener study ##ms py 80 well meas 21 invention up formula compounds mhz ##ile further sel inf dd ##ory ##ack ##ryst vari ##min ##ll ##ug ##hem ##epar ##arm ##ving ##ill 45 ##rough ##amples 37 ##get el nitro ##ove ##carb ##agn ##ication imp 23 low use ##ros ##ring following ##oac 201 car proced gl calc according prefer ##tical ##ycl through ##ons high ether cond ##lec ##cept containing control filtr ##ust carboxyl ##iti sur trif ##ood treat ##benz dil white val 28 ##ption same cooled tert cou ##phenyl ##ake ##ech ##ometh trifluor ##hib ##aturated ##ole ##chlor ##ants sequ ##ired cdcl has separ hydroxy ##ice 70 combined salt 00 id tetrahydro ##tur than ##ail ester performed 90 heated ##rain 26 ##ude evaporated when alkyl day ##med above 95 ##iss ##stem ##ility deg ##amino ##ases ##are 27 been sa followed ##led incre exper dep 400 ##methyl ##co saturated 32 29 ##ual ##opropyl removed stirring dihydro 75 sec fun ##ang mater dry phase sulfate ##ick equ 4h level ##hyd 05 ##omethyl ##ization non supp ##oci hydrogen ##br model fr patients ##ost ##ke treatment found °c compar ##itions ##mon 48 process ##der specific ##cer thi ##raz typ ##ects system 33 ##ange heat ##mun material piper ##iment ##cc etoac crude ##fore dec gra treated signific sl hydrochlor inhib deter dur if ##ser ##ences met synt ##omethane their afford 31 vacuo medium both cat bu ##onic dmso 36 procedure def ##ues groups brine rat ##anc three inv cryst po 34 phosph det flas antibod num ##wise ##ently pep ##ock ##mal hal 55 ##ably hexane anhydro fir susp allow ##ously ##ough cook off ##rap anhydrous char ##ulated ##tal ##anes ##ellow ##to ##night 42 ii dichloromethane set overnight lar ##ulation ##cip 38 ##ophenyl benzyl yellow hum associ expression function ##ension ##ink ##ified drop 300 ##pm ##entif ##ale sm ##ogen ethanol gene kn vol simil ##ram stat appro ma ##ath subj ##bs cent test ##ric ##ner magn similar tol ##vers table significant ##lux 65 diluted collec based substituted ##ucle mem ##etic ##rile ##inal prim first ##inding measur provid results 01 activity ##ma prot during mice ##ano ##hex ##itrile ##medi stand dise synthes benzo ##acter heter ##ments previ pe reflux ##cr embod collected 43 ##ork cul ##av rt second end ##rown 39 41 thf cyclo lc ##osp incub ##other bromo ##up ##ew 44 ice star how diox ##ective 500 determ ##tern 85 cdcl3 any ##so4 fluoro ##ute ele ##ately 46 amou samples atom rem ##ave ris inhibit ##ions ##ize nor immun ##azole alk number ##ten preparation der studies ##uran nitrogen total hr pur assay had while particip 52 obser light show buffer ##iments ##tim repres dr 47 ##ines ##velop tar gre pa ##10 they 02 struc ##itive μl include ##esium human preferably compos 78 72 ##carbonyl sample here fact oxo refer ##cipit ##minis mul op ##alkyl develop molec pow nh lab dna shown sk ##plc indic our bas adminis identif so 56 ##ited having 53 49 phen ##aly ##alth ##ectiv hcl 199 mar lim different tes ##onate some carboxylic selected ##int 54 conf least chem tolu ##cm only ##onitrile place 51 96 repor will wherein before anim ##ocy pyridin small including cm ##orph pharm ##dr ##ethoxy dropwise concentration conditions mo those ##ould figure times appl its 99 analy separated ##xim 58 large ##ps te within liqu hplc ##atory like ##ness dire pyraz ##tide ##less desired pyrrol ppm ##atic ##inyl poly bow pan 62 precipit remain without health ##ible target amount ##fluor 57 esi 98 weight ol brown tiss ##old ep cur ##ator ##ie ##ination suspension 64 ##ins isol another ##ages ##2o 6h 03 pyrim thus 63 degree ##ever ##inol polym assess ##ish liquid ##ortion av ir ##val az general ##ivid induc inj gly nucle days color usa clin cre carbonate 68 magnesium bowl cataly ##oph meoh 150 levels cancer trifluoromethyl main ##ology individ compr che tum allowed cle ##zed ##xt ##ydr methods ##istic del ##ger ##use ##ability standard 04 ##aking bis distil ##assium ##yn 59 bec ##anti lower however ##furan pyridine 67 rad top disease ##echn mass line purification 66 plas ##eng intermedi potassium ##ci ##ables filtration ##ple ##ological remove filtrate free ##ativ grad associated 61 ##its il ##ept ##omer dist acetic type ##ically ch2 88 ##bl effect cap diethyl ##ful ##ential 82 toluene 92 chloroform ap adj manner ##ks ##ross vacuum ##dehyd ##gar antibody ##ides volum mut multi 76 97 mel sing 06 ##ectively 94 ##struc path imid mean 08 you provide ##utic ##cin parti ##thi measured 73 prob ##ade additional tetrahydrofuran ##enyl vis loc 84 ##oyl measure ##dehyde sof calculated represent ##yclo dcm d6 herein 74 dem μm most previously oven micro presence 83 dmf particular iod ##tid fraction ##ethylamine ##eg compared ##ouse ##sequ corre ##iod 69 examples rate amine 86 binding ##ency 77 fe ed ##cl2 07 ##ml 93 year 71 hydroxide ##cess ##osed bel intermediate experiment ##osis single ##uting 87 observed occ determined ##ulfonyl therap propyl hydrochloride 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