1.2 => fil detherm => s polymeri!ation# L1 6 POLYMERI!ATION# => d 1- hit
1.3 => fil gme => s xenon (l) fluor? 124 XENON 7521 FLUOR? L1 15 XENON (L) FLUOR? => d 1-5 trial
1.4
=> fil bei
=> s aspirin# or (a!etyl sali!yl## (w)(saeure or acid))
339 ASPIRIN#
251703 A!ETYL
4080 SALI!YL##
11 A!ETYL SALI!YL##
(A!ETYL(W)SALI!YL##)
13924 SAEURE
2630520 ACID
9 A!ETYL SALI!YL## (W)(SAEURE OR ACID)
L1 347 ASPIRIN# OR (A!ETYL SALI!YL## (W)(SAEURE OR ACID))
=> s aspirin/cn
L2 1 ASPIRIN/CN
=> d ide
L2 ANSWER 1 OF 1 COPYRIGHT 1996 Beilstein
Beilstein Reg. No. (BRN): 779271 Beilstein
Molecular Formula (MF): C9 H8 O4
Chemical Name (CN): 2-acetoxy-benzoic acid
2-Acetoxy-benzoesaeure
Synonym (SY): Acetylsalicylsaeure; acetylsalicylic acid;
salicylic acid acetate; 2-(acetyloxy)-benzoic
acid; O-acetyl-salicylic acid;
***aspirin***
Autonom Name (AUN): 2-acetoxy-benzoic acid
=> s l1 or salicylic acid acetate
L3 347 L1 OR SALICYLIC ACID ACETATE
=> s l3 or acetoxy-benzoic acid
L4 1141 L3 OR ACETOXY-BENZOIC ACID
=> s l4 or 2-Acetoxy-benzoesaeure
L5 1181 L4 OR 2-ACETOXY-BENZOESAEURE
=> s l5 or Acetylsalicylsaeure
L6 1197 L5 OR ACETYLSALICYLSAEURE
=> s l6 or acetylsalicylic acid
L7 1353 L6 OR ACETYLSALICYLIC ACID
=> s l7 or acetyloxy benzoic acid
L8 1353 L7 OR ACETYLOXY BENZOIC ACID
1.5 => fil chemin => e mulzer /au E1 1 MULVEY, D M/AU E2 1 MULZAC, D/AU E3 0 --> MULZER/AU E4 24 MULZER, J/AU E5 1 MUMFORD, R A/AU E6 1 MUMLADZE, E A/AU E7 1 MUMPER, M W/AU E8 2 MUN, G S/AU E9 2 MUN, K R/AU E10 2 MUNAKATA, H/AU E11 5 MUNAKATA, M/AU E12 3 MUNAKATA, Y/AU => s e4 L1 24 "MULZER, J"/AU => sel l1 1- jt E11 THROUGH E20 ASSIGNED => d sel e11 - e20 E11 7 LIEBIGS ANN. CHEM./JT E12 6 ANGEW. CHEM./JT E13 5 TETRAHEDRON LETT./JT E14 2 J. AM. CHEM. SOC./JT E15 2 TETRAHEDRON/JT E16 1 ASYMMETRY/JT E17 1 HETEROCYCLES/JT E18 1 J. HETEROCYCL. CHEM./JT E19 1 J. ORG. CHEM./JT E20 1 SYNTHESIS/JT
1.6
=>fil chemin
=> s (michael addition or michael rea!tion)
701 MICHAEL
16266 ADDITION
380 MICHAEL ADDITION
(MICHAEL(W)ADDITION)
701 MICHAEL
20945 REA!TION
95 MICHAEL REA!TION
(MICHAEL(W)REA!TION)
L1 464 (MICHAEL ADDITION OR MICHAEL REA!TION)
1.7 d his ful d cost ful
2.4 => fil bei => s l1 ful FULL SEARCH INITIATED FULL SCREEN SEARCH COMPLETED - 13177 TO ITERATE 80.6% PROCESSED 10624 ITERATIONS 7120 ANSWERS 100.0% PROCESSED 13177 ITERATIONS 8744 ANSWERS SEARCH TIME: 00.00.46 L2 8744 SEA SSS FUL L1 => s l2 and xanthin#/cn 4 XANTHIN#/CN L3 3 L2 AND XANTHIN#/CN
- Adenin hat nur an einer der bezeichneten Stellen einen Stickstoff- (bzw. Sauerstoff-) Substituenten.
2.5 => fil bei => s l1 css ful FULL SEARCH INITIATED FULL SCREEN SEARCH COMPLETED - 581 TO ITERATE 100.0% PROCESSED 581 ITERATIONS 10 ANSWERS SEARCH TIME: 00.00.05 L2 10 SEA CSS FUL L1 => fil gme => s l1 css ful FULL SEARCH INITIATED FULL SCREEN SEARCH COMPLETED - 32 TO ITERATE 100.0% PROCESSED 32 ITERATIONS 3 ANSWERS SEARCH TIME: 00.00.03 L3 3 SEA CSS FUL L1
2.6 => fil gme => s l1 sss ful FULL SEARCH INITIATED FULL SCREEN SEARCH COMPLETED - 9247 TO ITERATE 100.0% PROCESSED 9247 ITERATIONS 864 ANSWERS SEARCH TIME: 00.00.16 L2 864 SEA SSS FUL L1 => s l1 css ful FULL SEARCH INITIATED FULL SCREEN SEARCH COMPLETED - 9247 TO ITERATE 100.0% PROCESSED 9247 ITERATIONS 337 ANSWERS SEARCH TIME: 00.00.16 L3 337 SEA CSS FUL L1 => s l1 fam ful FULL SEARCH INITIATED FULL SCREEN SEARCH COMPLETED - 1546 TO ITERATE 100.0% PROCESSED 1546 ITERATIONS 291 ANSWERS SEARCH TIME: 00.00.05 L4 291 SEA FAM FUL L1 => s l1 exa ful FULL SEARCH INITIATED FULL SCREEN SEARCH COMPLETED - 101 TO ITERATE 100.0% PROCESSED 101 ITERATIONS 33 ANSWERS SEARCH TIME: 00.00.02 L5 33 SEA EXA FUL L1
- Mit sss werden Strukturen mit oder ohne Substitutionen an beliebiger Stelle gefunden; mit css werden Strukturen mit Substitution an der bezeichneten Stelle gefunden; mit fam wird sowohl die exakte Struktur als auch deren Salze bzw. Mehrkomponentensysteme gefunden; mit exa wird die exakte Struktur gefunden.
- Mit exa werden auch Stereoisomere und Isotopenverbindungen gefunden.
=> e benzidin/cn ... E3 1 --> BENZIDIN/CN ... s e3 L1 1 BENZIDIN/CN => d ide fa ... => d nmra ctnmr dm msus ctmag ... => d slb
=> s 10/c and 21/h and 32/atc and a7/pg
371640 10/C
213272 21/H
192559 32/ATC
1787187 A7/PG
L42 325 10/C AND 21/H AND 32/ATC AND A7/PG
=> e methyl/cns ... => e cyclopenten/cns ... => e cyclopentene/cns ... => e dihydro/cns ... => e phenanthren/cns ... => e phenanthrene/cns ... => s (methyl(l)cyclopenten#(l)dihydro(l)phenanthren#)/cns ... => d ide
=> set unit bp=c
SET COMMAND COMPLETED
=> set unit bp.p=hpa
SET COMMAND COMPLETED
=> s al!ohol/cns and 97-98/bp (p) 1013-1014/bp.p
3285 AL!OHOL/CNS
26561 97 C - 98 C /BP
19272 1013 HPA - 1014 HPA /BP.P
360 97 C - 98 C /BP (P) 1013 HPA - 1014 HPA /BP.P
L1 4 AL!OHOL/CNS AND 97 C - 98 C /BP (P) 1013 HPA - 1014 HPA /B
P.P
=> d l1 cn hit
=> e anilin/cn
...
E3 3 --> ANILIN/CN
E4 1 ANILIN (1 MOL)/CN
...
s e4
L1 1 ANILIN (1 MOL)/CN
d brn
L1 ANSWER 1 OF 1 COPYRIGHT 1996 Beilstein
Beilstein Reg. No. (BRN): 605631 Beilstein
=> s indigo/cn and 605631/pre.sm
1 INDIGO/CN
18580 605631/PRE.SM
L2 1 INDIGO/CN AND 605631/PRE.SM
=> d ide hit
L2 ANSWER 1 OF 1 COPYRIGHT 1996 Beilstein
Beilstein Reg. No. (BRN): 88275 Beilstein
...
=> s l1 and 88275/rea.pro
96 88275/REA.PRO
L3 0 L3 AND 88275/REA.PRO
=> s vanadium/cn L1 5 VANADIUM/CN => s v/mf L2 5 V/MF => d 1-5 idetab
- Es werden verschiedene Modifikationen und Isotope des Elements gefunden.
=> s be2feo10si2y2/m L1 2 BE2FEO10SI2Y2/MF => d 1- cn
=> e vanadinit/cn
...
E3 0 --> VANADINIT/CN
E4 1 VANADINIT (GERM.)/CN
E5 1 VANADINITE/CN
...
=> s e4-e5
1 "VANADINIT (GERM.)"/CN
1 VANADINITE/CN
L1 1 ("VANADINIT (GERM.)"/CN OR VANADINITE/CN)
=> d ide
=> s clo12pb5v3/mf
L2 3 CLO12PB5V3/MF
=> d 1- ide
=> s "pb5(vo4)3cl"/lsf
L3 1 "PB5(VO4)3CL"/LSF
=> d ide
=> s l1 exa ful FULL SEARCH INITIATED FULL SCREEN SEARCH COMPLETED - 1 TO ITERATE 100.0% PROCESSED 1 ITERATIONS 1 ANSWERS SEARCH TIME: 00.00.05 L1 1 SEA SSS FUL L23 => d fa L1 ANSWER 1 OF 1 GMELIN COPYRIGHT 1996 GMELIN Field Availability: Code |Field Name |Occur. ========+=======================================================+====== ... | ... | ... CPD |Crystal Property Description |1 ... | ... | ... REA |Reaction |1 ... | ... | ... => d ide cpd rea => sel l1 grn E1 THROUGH E1 ASSIGNED => s e1/rea.pro L2 1 1037176/REA.PRO => d hit
=> s cu/mac.w (p) major/mac.w and p/mac.w (p) 0.01-0.5/mac.w and alloy/fn
3101 CU/MAC.W
33369 MAJOR/MAC.W
1455 CU/MAC.W (P) MAJOR/MAC.W
847 P/MAC.W
4773 0.01-0.5/MAC.W
320 P/MAC.W (P) 0.01-0.5/MAC.W
54225 ALLOY/FN
L1 37 CU/MAC.W (P) MAJOR/MAC.W AND P/MAC.W (P) 0.01-0.5/MAC.W AN
D ALLOY/FN
=> s l1 and sn/mac.w
2590 SN/MAC.W
L2 11 L25 AND SN/MAC.W
=> d 1- mactab
=> str :gra r6 :nod 1 3 5 n :bon 1-2 3-4 5-6 d :bon 2-3 4-5 6-1 s :att 2 s o :att 4 s o :att 6 s o :dis :rol 1 pro :end L1 STRUCTURE CREATED => s l1 ful ... L34 10 SEA SSS FUL L32 ( 20 REACTIONS) => d scan
=> s ziegler(a)thorpe
21 ZIEGLER
16 THORPE
L3 8 ZIEGLER(A)THORPE
=> d 1- ab cbib
=> str :gra r5 :bon 3-4 d :nod 2 o :att 1 d o :att 3 d o :bon 3-4 2-3 1-2 1-5 s :bon 4-5 d :rol 1 rrt :dis ... :end L1 STRUCTURE CREATED => s l1 css ful ... L2 159 SEA CSS FUL L1 ( 578 REACTIONS) => d scan ... => str l1 :rol 1 rct :end L3 STRUCTURE CREATED => s l3 css ful ... L4 147 SEA CSS FUL L3 ( 533 REACTIONS) => str l1 :rol 1 rgt :end L5 STRUCTURE CREATED => s l5 css ful ... L6 12 SEA CSS FUL L5 ( 45 REACTIONS)
=> s decane/sol.cn L1 13 DECANE/SOL.CN
=> str :gra r6 :att 1 se cl :att 2 s no2 :bon 1-7 2-3 4-5 6-1 s :bon 1-2 3-4 5-6 d :cop 1 :del 15 :att 11 s nh2 :rol 1 rrt, rol 9 pro :map 1 11, map 2 9 :dis sia ... :end L1 STRUCTURE CREATED s l1 ful ... L26 3 SEA SSS FUL L24 ( 11 REACTIONS) d 1- fhit
=> s thiol/rrt (l) thioester/pro.kw (a) ydp>95
1478 THIOL/RRT
586 THIOESTER/PRO.KW
9507 YDP>95 %
L1 6 THIOL/RRT (L) THIOESTER/PRO.KW (A) YDP>95 %
=> str
:gra r6
:att 3 r4
:att 9 r6
:att 6 s o
:att 14 s o
:att 17 se ch3, att 18 se ch3
:nod 8 10 s
:nod 7 9 p
:att 7 s d
:att 9 s d
:bon 7-21 9-22 2-3 4-5 6-1 12-13 14-15 16-11 d
:bon 1-2 3-4 5-6 7-8 8-9 9-10 10-7 3-7 9-11 11-12 13-14 15-16 s
:rol 1 rrt
:end
L1 STRUCTURE CREATED
=> s l1 css ful
...
L2 165 SEA CSS FUL L1 ( 1030 REACTIONS)
=> s l2 or lawesson?/npro
140 LAWESSON?/NPRO
L3 169 L48 OR LAWESSON?/NPRO
=> e benzoic/cn ... E4 1 BENZOIC ACID/CN ... => s e4 L1 1 "BENZOIC ACID"/CN => d allms
=> Uploading niclosam.str L1 STRUCTURE UPLOADED => run che l1 si *** SPECINFO CHEMICAL STRUCTURE SEARCH *** NUMBER OF HITS :1 L2 RUN STATEMENT CREATED ENTER TYPE OF SEARCH (END) :end => d ide allms
=> run ed ir
*** SPECINFO SPECTRUM EDITOR ***
:1314,90,25
:1370,72,15
:1489,99,30
:1539,87,40
:1608,76,15
:sav
L1 RUN STATEMENT CREATED
=> run get l1 ir
*** SPECINFO SPECTRUM SIMILARITY SEARCH ***
ANS NO SPEC NO ACC NO SIMILARITY
=======+=======+==========+==========
1 2 55468417 47
2 1 32665199 46
1 1 55468417 45
3 1 70022845 43
4 1 47413137 42
5 1 40370353 41
6 1 18233020 40
7 1 71940953 40
8 1 50475641 40
9 1 94578329 39
10 1 49163537 39
11 1 75036889 39
12 1 47235533 39
13 1 97936033 39
14 1 11583191 39
L2 RUN STATEMENT CREATED
=> sel l5 1- srn
E1 THROUGH E36 ASSIGNED
=> s e1-e36 and 1/elr.ch and 8/elr.cn
1 STCC-11583-191/SRN
1 STCC-14867-427/SRN
1 STCC-18233-020/SRN
1 STCC-21171-675/SRN
1 STCC-23962-762/SRN
1 STCC-32665-199/SRN
1 STCC-36230-755/SRN
1 STCC-37646-469/SRN
1 STCC-40370-353/SRN
1 STCC-40436-245/SRN
1 STCC-45700-933/SRN
1 STCC-47054-653/SRN
1 STCC-47235-533/SRN
1 STCC-47413-137/SRN
1 STCC-49163-537/SRN
1 STCC-50475-641/SRN
1 STCC-55468-417/SRN
1 STCC-64095-585/SRN
1 STCC-64479-157/SRN
1 STCC-69554-653/SRN
1 STCC-69601-221/SRN
1 STCC-70022-845/SRN
1 STCC-70628-937/SRN
1 STCC-71940-953/SRN
1 STCC-72587-369/SRN
1 STCC-75036-889/SRN
1 STCC-76177-513/SRN
1 STCC-82922-049/SRN
1 STCC-84053-425/SRN
1 STCC-87995-321/SRN
1 STCC-89124-161/SRN
1 STCC-94178-425/SRN
1 STCC-94578-329/SRN
1 STCC-97936-033/SRN
1 STCC-99036-961/SRN
1 STCC-99472-473/SRN
9255 1/ELR.CH
3581 8/ELR.CN
L6 1 (STCC-11583-191/SRN OR STCC-14867-427/SRN OR STCC-18233-02
0/SRN OR STCC-21171-675/SRN OR STCC-23962-762/SRN OR STCC-
32665-199/SRN OR STCC-36230-755/SRN OR STCC-37646-469/SRN
OR STCC-40370-353/SRN OR STCC-40436-245/SRN OR STCC-45700-
933/SRN OR STCC-47054-653/SRN OR STCC-47235-533/SRN OR STC
C-47413-137/SRN OR STCC-49163-537/SRN OR STCC-50475-641/SR
N OR STCC-55468-417/SRN OR STCC-64095-585/SRN OR STCC-6447
9-157/SRN OR STCC-69554-653/SRN OR STCC-69601-221/SRN OR S
TCC-70022-845/SRN OR STCC-70628-937/SRN OR STCC-71940-953/
SRN OR STCC-72587-369/SRN OR STCC-75036-889/SRN OR STCC-76
177-513/SRN OR STCC-82922-049/SRN OR STCC-84053-425/SRN OR
STCC-87995-321/SRN OR STCC-89124-161/SRN OR STCC-94178-42
5/SRN OR STCC-94578-329/SRN OR STCC-97936-033/SRN OR STCC-
99036-961/SRN OR STCC-99472-473/SRN) AND 1/ELR.CH AND 8/EL
R.CN
=> d ide
=>
Uploading spec.str
L1 STRUCTURE UPLOADED
=> run specal l1 all c
*** CALCULATION OF NMR SPECTRUM LINE VALUES ***
CHARGED STRUCTURES EXCLUDED - POLAR SOLVENTS EXCLUDED
ATOM NO. MEAN STD. DEV. MULTIPL. HITS
(PPM) (PPM)
==========+===========+=============+===========+===============
1 125.34 0.70 S (INTERPOLATED)
2 138.93 2.26 D (INTERPOLATED)
3 144.74 5.94 D (INTERPOLATED)
5 148.30 0.30 S (INTERPOLATED)
6 121.05 4.05 D (INTERPOLATED)
7 165.15 0.05 S ( 2 LINES )
9 61.22 0.81 T ( 164 LINES )
10 14.09 0.41 Q ( 2900 LINES )
12 165.00 0.00 S ( 1 LINE )
14 62.12 0.72 T ( 15 LINES )
15 14.09 0.41 Q ( 2900 LINES )
L2 RUN STATEMENT CREATED
ENTER NODE NUMBER (END) :10
ATOM NUMBER : 10
MULTIPLICITY : Q
HOSE CODE : C(O/C$/C)
NO. OF LINE VALUES : 2900
NO. OF STRUCTURES : 2070
MEAN, STANDARD DEVIATION : 14.1+/- 0.4 PPM
RANGE : 8.9 - 20.1 PPM
ENTER SD,DR,CL,SE,R (END):sd
INTERVAL HITS
(PPM)
-----------------+------
8 - 9 1
9 - 10 0
10 - 11 0
11 - 12 11
12 - 13 31
13 - 14 992
14 - 15 1854
15 - 16 7
16 - 17 0
17 - 18 2
18 - 19 0
19 - 20 1
20 - 21 1
ENTER SD,DR,CL,SE,R (END):dr
ENTER LOWER VALUE (?) :13
ENTER UPPER VALUE (?) :15
NO. OF LINE VALUES : 2846
NO. OF STRUCTURES : 2044
MEAN, STANDARD DEVIATION : 14.1+/- 0.3 PPM
RANGE : 13.0 - 15.0 PPM
ENTER SD,DR,CL,SE,R (END):sd
INTERVAL HITS
(PPM)
-----------------+------
13.0 - 13.5 113
13.5 - 14.0 879
14.0 - 14.5 1733
14.5 - 15.0 121
ENTER SD,DR,CL,SE,R (END):.
=> run coupcal l1 1 7 *** CALCULATION OF NMR COUPLING CONSTANTS *** COUPLING ATOM NUMBERS : 1 - 7 COUPLING NUCLEI : C - C COUPLING CODE : 1J(C,C)0(.)=OO,*C*C NUMBER OF COUPLINGS : 28 NUMBER OF STRUCTURES : 22 MEAN, STANDARD DEVIATION : 72.1+/- 2.8 HZ RANGE : 65.0 - 75.8 HZ ENTER SD, DR OR CL (END) :.
=> e piperidine+all/cn
E1 MF C5 H11 N/CN
E2 211 --> Piperidine/CN
E3 RN 110-89-4/CN
UF Azacyclohexane
UF Hexahydroazine
UF Hexahydropyridine
********* END *********
=> s piperidine/cn and vs/prop
211 PIPERIDINE/CN (1 TERM)
16305 VS/PROP
L1 3 PIPERIDINE/CN AND VS/PROP
=> d ide bib tbl
=> s nilsson?/au and acta chem scand/jt and 1970-1979/py
14 NILSSON?/AU
34 ACTA CHEM SCAND/JT
(ACTA CHEM SCAND/JT)
6718 1970-1979/PY
L1 3 NILSSON?/AU AND ACTA CHEM SCAND/JT AND 1970-1979/PY
=> sel l1 1- table
E1 THROUGH E3 ASSIGNED
=> s e1-e3
2 9-1541/RACC
1 9-1774/RACC
5 9-2059/RACC
L2 8 (9-1541/RACC OR 9-1774/RACC OR 9-2059/RACC)
=> d 1- tbl bib
=> s c/els and o/els and (t1 or t2 or t3)/pg and 3/elc and i10/syst
263012 C/ELS
(C/ELS)
169103 O/ELS
(O/ELS)
3831 T1/PG
1711 T2/PG
879 T3/PG
166441 3/ELC
20797 I10/SYST
L1 9 C/ELS AND O/ELS AND (T1 OR T2 OR T3)/PG AND 3/ELC AND
I10/SYST
BESSERE MÖGLICHKEIT:
=> s carbonyl/cns and (t1 or t2 or t3)/pg and i10/syst
45 CARBONYL/CNS
3831 T1/PG
1711 T2/PG
879 T3/PG
20797 I10/SYST
L2 8 CARBONYL/CNS AND (T1 OR T2 OR T3)/PG AND I10/SYST
=> s den/prop (p) 25c/temp (p) 1013hpa/pres and o10/syst
27221 DEN/PROP
159833 TEMP/PROP
51633 25C/UNIT1
46275 25C/TEMP
(TEMP/PROP(S)25C/UNIT1)
21981 PRES/PROP
739 1013HPA/UNIT2
474 1013HPA/PRES
(PRES/PROP(S)1013HPA/UNIT2)
23 DEN/PROP (P) 25C/TEMP (P) 1013HPA/PRES
117459 O10/SYST
L1 16 DEN/PROP (P) 25C/TEMP (P) 1013HPA/PRES AND O10/SYST
=> d qrd
=> s xe/els (t) f/els and nc >=2
443 Xe/ELS
(Xe/ELS)
16222 F/ELS
(F/ELS)
23 Xe/ELS (T) F/ELS
158308 NC >=2
L1 4 Xe/ELS (T) F/ELS AND NC >=2
=> d 1- ide bib tbl
=> fil kkf
...
=> s (high pressure or hochdruck)(w)(fluessigchromatograph? or liquid
chromatograph?) or hplc or hochdruckfluessigchromatograph?
8623 HIGH
2539 PRESSURE
585 HIGH PRESSURE
(HIGH(W)PRESSURE)
861 HOCHDRUCK
882 FLUESSIGCHROMATOGRAPH?
5481 LIQUID
6982 CHROMATOGRAPH?
283 LIQUID CHROMATOGRAPH?
(LIQUID(W)CHROMATOGRAPH?)
23 (HIGH PRESSURE OR HOCHDRUCK)(W)(FLUESSIGCHROMATOGRAPH? OR
LIQUID CHROMATOGRAPH?)
416 HPLC
17 HOCHDRUCKFLUESSIGCHROMATOGRAPH?
L1 444 (HIGH PRESSURE OR HOCHDRUCK)(W)(FLUESSIGCHROMATOGRAPH? OR
LIQUID CHROMATOGRAPH?) OR HPLC OR HOCHDRUCKFLUESSIGCHROMAT
OGRAPH?
=> d bib ab
=> fil vtb
...
=> s virusinfe!t##### or ((virus## or viral##) (s) infe!t#####) (nots)
hiv not aids
6 VIRUSINFE!T#####
40 VIRUS##
12 VIRAL##
85 INFE!T#####
10 HIV
6 ((VIRUS## OR VIRAL##) (S) INFE!T#####) (NOTS) HIV
139 AIDS
L1 11 VIRUSINFE!T##### OR ((VIRUS## OR VIRAL##) (S) INFE!T#####)
(NOTS) HIV NOT AIDS
=> d bib ab
=> fil bei
...
=> str
:gra r6
:bon 1-2 3-4 5-6 d
:bon 2-3 4-5 6-1 s
:att 1 x se
:att 3 g1 se
:var g1=h/ak
:gra c1
:nod 9 no2
:vpa 9-4/5
:end
L1 STRUCTURE CREATED
=> s l1 css ful
...
L2 35 SEA CSS FUL L1
=> d
=> fil bei ... => str :gra c2 :bon 1-2 de :att 1 me se v10 :att 1 x se v8 :att 2 x se v2 :att 2 et se v4 :ste all flat :end L1 STRUCTURE CREATED => str l1 :ste all vis :end L2 STEREO STRUCTURE CREATED => s l1 ful FULL SEARCH INITIATED SCREENING FULL SCREEN SEARCH COMPLETED - 25683 TO ITERATE 41.3% PROCESSED 10607 ITERATIONS 0 ANSWERS 73.1% PROCESSED 18762 ITERATIONS 1 ANSWERS 89.4% PROCESSED 22954 ITERATIONS 3 ANSWERS 100.0% PROCESSED 25683 ITERATIONS 6 ANSWERS SEARCH TIME: 00.01.23 L3 6 SEA SSS FUL L1 => s l2 ful subset=l3 FULL SUBSET SEARCH INITIATED FULL SUBSET SCREEN SEARCH COMPLETED - 6 TO ITERATE 100.0% PROCESSED 6 ITERATIONS 2 ANSWERS SEARCH TIME: 00.00.03 L4 2 SEA SUB=L3 SSS FUL L2 => d 1-
9.1
=> s de4327838/pn
L1 1 DE4327838/PN
(DE4327838/PN)
=> d
9.2
=> s automat? (a) pipett?
3732 AUTOMAT?
25 PIPETT?
L1 3 AUTOMAT? (A) PIPETT?
=> d 1 ti tt abs gi
9.3
=> e allis-chalmers/pa
E1 37 ALLIED-SIGNAL INC/PA
E2 14 ALLIS/PA
E3 0 --> ALLIS-CHALMERS/PA
E4 8 ALLIS-CHALMERS CORP/PA
E5 4 ALLIS-CHALMERS MFG CO/PA
...
=> s e4-e5
8 "ALLIS-CHALMERS CORP"/PA
4 "ALLIS-CHALMERS MFG CO"/PA
L1 12 ("ALLIS-CHALMERS CORP"/PA OR "ALLIS-CHALMERS MFG CO"/PA)
=> sel l1 1- paco
E1 THROUGH E1 ASSIGNED
=> s e1
L1 12 ALCM/PACO
(ALCM/PACO)
=> s l1 and 1980/py
3492 1980/PY
L2 1 L1 AND 1980/PY
=> d
9.4
=> s aspirin or (((acetyl? salicyl?) or acetylsalicyl?) (w) acid)
12 ASPIRIN
431 ACETYL?
93 SALICYL?
9 ACETYL? SALICYL?
(ACETYL?(W)SALICYL?)
5 ACETYLSALICYL?
6423 ACID
8 ((ACETYL? SALICYL?) OR ACETYLSALICYL?) (W) ACID
L1 18 ASPIRIN OR (((ACETYL? SALICYL?) OR ACETYLSALICYL?) (W)ACI
D)
=> s l1 and de/pc,ds
14006 DE/PC
9274 DE/DS
L2 7 L3 AND DE/PC,DS
=> d hit bib 1-
9.5
=> e bosch/pa
E1 1 BOS/PA
E2 3 BOSAI/PA
E3 224 --> BOSCH/PA
E4 1 BOSCH AG ROBERT/PA
E5 2 BOSCH FERNSEHANLAGEN GMBH/PA
E6 198 BOSCH GMBH ROBERT/PA
E7 1 BOSCH HAUSGERA ETE GMBH ROBERT/PA
E8 1 BOSCH K/PA
E9 1 BOSCH R/PA
E10 1 BOSCH SIEMENS AG/PA
E11 19 BOSCH SIEMENS HAUSGERAETE GMBH/PA
E12 1 BOSCH TELECOM OEFFENTLICHE VERMITTLUNGS/PA
=> s e4
L1 1 "BOSCH AG ROBERT"/PA
=> sel l1 paco 1
E1 THROUGH E1 ASSIGNED
=> s e1
L2 224 BOSC/PACO
(BOSC/PACO)
=> s l2 and (zimmer j)/in
1 (ZIMMER J)/IN
L3 1 L2 AND (ZIMMER J)/IN
d ti abs hit gi
9.6
=> e hoffmann/pa
E1 1 HOFFMAN S/PA
E2 1 HOFFMAN-LA ROCHE/PA
E3 47 --> HOFFMANN/PA
E4 1 HOFFMANN - LA ROCHE/PA
E5 1 HOFFMANN A/PA
E6 3 HOFFMANN D/PA
E7 1 HOFFMANN J/PA
E8 11 HOFFMANN LA ROCHE & CO AG F/PA
E9 1 HOFFMANN LA ROCHE & CO KG F/PA
E10 9 HOFFMANN LA ROCHE INC/PA
E11 2 HOFFMANN M/PA
E12 1 HOFFMANN S SCHUBERT H WIT/PA
=> s e8-e10
11 "HOFFMANN LA ROCHE & CO AG F"/PA
1 "HOFFMANN LA ROCHE & CO KG F"/PA
9 "HOFFMANN LA ROCHE INC"/PA
L1 18 ("HOFFMANN LA ROCHE & CO AG F"/PA OR "HOFFMANN LA ROCHE &
CO KG F"/PA OR "HOFFMANN LA ROCHE INC"/PA )
=> sel l1 paco 1-
E1 THROUGH E1 ASSIGNED
=> s e1
L2 38 HOFF/PACO
(HOFF/PACO)
=> sel l2 1- dc
E1 THROUGH E33 ASSIGNED
=> d sel e1-e10
E1 8 B05/DC
E2 7 B02/DC
E3 5 B00/DC
E4 5 J04/DC
E5 4 B03/DC
E6 4 S03/DC
E7 2 B04/DC
E8 2 C00/DC
E9 2 C02/DC
E10 2 D13/DC
=> e b05/dc
...
E3 850 --> B05/DC
E4 0 B05 Organics incl. arom., aliph., organometallics/DC
...
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