NO148554B - Analogifremgangsmaate til fremstilling av terapeutisk virksomme 1-(azacykliske aralkoksyfenyl)-2- eller -3-(bis-arylalkylamino)-alkaner - Google Patents
Analogifremgangsmaate til fremstilling av terapeutisk virksomme 1-(azacykliske aralkoksyfenyl)-2- eller -3-(bis-arylalkylamino)-alkaner Download PDFInfo
- Publication number
- NO148554B NO148554B NO772211A NO772211A NO148554B NO 148554 B NO148554 B NO 148554B NO 772211 A NO772211 A NO 772211A NO 772211 A NO772211 A NO 772211A NO 148554 B NO148554 B NO 148554B
- Authority
- NO
- Norway
- Prior art keywords
- layer
- image
- photoconductive
- thermoplastic
- exposure
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 41
- 150000001335 aliphatic alkanes Chemical class 0.000 title 1
- 230000001225 therapeutic effect Effects 0.000 title 1
- 239000000463 material Substances 0.000 claims description 58
- 239000002904 solvent Substances 0.000 claims description 25
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 19
- 229910052711 selenium Inorganic materials 0.000 claims description 19
- 239000011669 selenium Substances 0.000 claims description 19
- 238000010438 heat treatment Methods 0.000 claims description 15
- 230000000694 effects Effects 0.000 claims description 10
- 238000001816 cooling Methods 0.000 claims description 4
- 230000005686 electrostatic field Effects 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 230000008569 process Effects 0.000 abstract description 7
- 239000010410 layer Substances 0.000 description 217
- 229920001169 thermoplastic Polymers 0.000 description 62
- 239000004416 thermosoftening plastic Substances 0.000 description 62
- 239000007788 liquid Substances 0.000 description 52
- 238000007600 charging Methods 0.000 description 33
- 239000000758 substrate Substances 0.000 description 21
- 229920003023 plastic Polymers 0.000 description 20
- 239000004033 plastic Substances 0.000 description 19
- 238000000576 coating method Methods 0.000 description 16
- 239000011248 coating agent Substances 0.000 description 15
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 14
- 239000011230 binding agent Substances 0.000 description 14
- 238000011161 development Methods 0.000 description 13
- 230000003287 optical effect Effects 0.000 description 9
- 239000006185 dispersion Substances 0.000 description 8
- 239000011810 insulating material Substances 0.000 description 8
- 238000005286 illumination Methods 0.000 description 7
- 238000009413 insulation Methods 0.000 description 7
- 238000002844 melting Methods 0.000 description 7
- 239000011787 zinc oxide Substances 0.000 description 7
- 230000008859 change Effects 0.000 description 5
- 230000000994 depressogenic effect Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000012188 paraffin wax Substances 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 239000012815 thermoplastic material Substances 0.000 description 5
- 239000004793 Polystyrene Substances 0.000 description 4
- 230000009471 action Effects 0.000 description 4
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 4
- 238000004040 coloring Methods 0.000 description 4
- 238000007786 electrostatic charging Methods 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 229920002223 polystyrene Polymers 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 3
- YGUMVDWOQQJBGA-VAWYXSNFSA-N 5-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-[(e)-2-[4-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound C=1C=C(\C=C\C=2C(=CC(NC=3N=C(N=C(NC=4C=CC=CC=4)N=3)N3CCOCC3)=CC=2)S(O)(=O)=O)C(S(=O)(=O)O)=CC=1NC(N=C(N=1)N2CCOCC2)=NC=1NC1=CC=CC=C1 YGUMVDWOQQJBGA-VAWYXSNFSA-N 0.000 description 3
- 229910001369 Brass Inorganic materials 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000010951 brass Substances 0.000 description 3
- 238000007598 dipping method Methods 0.000 description 3
- 230000005684 electric field Effects 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000006698 induction Effects 0.000 description 3
- 239000012212 insulator Substances 0.000 description 3
- 239000011229 interlayer Substances 0.000 description 3
- 239000003350 kerosene Substances 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000003209 petroleum derivative Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 3
- 229910001887 tin oxide Inorganic materials 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 235000013871 bee wax Nutrition 0.000 description 2
- 239000012166 beeswax Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 238000003618 dip coating Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 230000020169 heat generation Effects 0.000 description 2
- 239000000976 ink Substances 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000615 nonconductor Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 230000004304 visual acuity Effects 0.000 description 2
- 150000005072 1,3,4-oxadiazoles Chemical class 0.000 description 1
- YOKGFEBGKOKPBX-UHFFFAOYSA-N 4-[3-(4-aminophenyl)-1h-1,2,4-triazol-5-yl]aniline Chemical class C1=CC(N)=CC=C1C1=NNC(C=2C=CC(N)=CC=2)=N1 YOKGFEBGKOKPBX-UHFFFAOYSA-N 0.000 description 1
- UZGVMZRBRRYLIP-UHFFFAOYSA-N 4-[5-[4-(diethylamino)phenyl]-1,3,4-oxadiazol-2-yl]-n,n-diethylaniline Chemical compound C1=CC(N(CC)CC)=CC=C1C1=NN=C(C=2C=CC(=CC=2)N(CC)CC)O1 UZGVMZRBRRYLIP-UHFFFAOYSA-N 0.000 description 1
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical class C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 229920006387 Vinylite Polymers 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- CJOBVZJTOIVNNF-UHFFFAOYSA-N cadmium sulfide Chemical compound [Cd]=S CJOBVZJTOIVNNF-UHFFFAOYSA-N 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000010205 computational analysis Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000005405 multipole Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- -1 polyethylene terephthalate Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- 229920006352 transparent thermoplastic Polymers 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000001429 visible spectrum Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/30—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D215/14—Radicals substituted by oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/699,017 US4091103A (en) | 1976-06-23 | 1976-06-23 | Quinolyl or isoquinolyl-lower-alkoxy-phenylene-amino derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO772211L NO772211L (no) | 1977-12-27 |
| NO148554B true NO148554B (no) | 1983-07-25 |
Family
ID=24807584
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO772211A NO148554B (no) | 1976-06-23 | 1977-06-22 | Analogifremgangsmaate til fremstilling av terapeutisk virksomme 1-(azacykliske aralkoksyfenyl)-2- eller -3-(bis-arylalkylamino)-alkaner |
Country Status (25)
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7487986B2 (en) * | 2002-10-16 | 2009-02-10 | 89908, Inc. | Retractable vehicle step |
| US9212127B2 (en) | 2004-08-20 | 2015-12-15 | University Of Virginia Patent Foundation | T type calcium channel inhibitors |
| US9427429B2 (en) | 2010-03-01 | 2016-08-30 | Tau Therapeutics Llc | Cancer diagnosis and imaging |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3906110A (en) * | 1973-02-07 | 1975-09-16 | Ciba Geigy Corp | Antihypertensive {60 -(1-aralkylaminoalkyl)-aralkoxybenzyl alcohols |
-
1976
- 1976-06-23 US US05/699,017 patent/US4091103A/en not_active Expired - Lifetime
-
1977
- 1977-03-31 ZA ZA00771962A patent/ZA771962B/xx unknown
- 1977-04-25 US US05/790,530 patent/US4110457A/en not_active Expired - Lifetime
- 1977-06-15 CY CY1167A patent/CY1167A/xx unknown
- 1977-06-15 GB GB25007/77A patent/GB1561516A/en not_active Expired
- 1977-06-18 DE DE19772727387 patent/DE2727387A1/de not_active Withdrawn
- 1977-06-20 GR GR53746A patent/GR82332B/el unknown
- 1977-06-20 NL NL7706780A patent/NL7706780A/xx unknown
- 1977-06-21 IL IL52359A patent/IL52359A/xx unknown
- 1977-06-21 FR FR7718973A patent/FR2355833A1/fr active Granted
- 1977-06-21 CA CA281,031A patent/CA1085404A/en not_active Expired
- 1977-06-21 PT PT66689A patent/PT66689B/pt unknown
- 1977-06-21 ES ES459963A patent/ES459963A1/es not_active Expired
- 1977-06-22 JP JP7340477A patent/JPS52156871A/ja active Pending
- 1977-06-22 NZ NZ184457A patent/NZ184457A/xx unknown
- 1977-06-22 DK DK276877A patent/DK276877A/da not_active Application Discontinuation
- 1977-06-22 BE BE178665A patent/BE855975A/xx not_active IP Right Cessation
- 1977-06-22 ZA ZA00773744A patent/ZA773744B/xx unknown
- 1977-06-22 FI FI771960A patent/FI771960A/fi not_active Application Discontinuation
- 1977-06-22 AT AT439577A patent/AT355575B/de not_active IP Right Cessation
- 1977-06-22 AU AU26327/77A patent/AU513828B2/en not_active Expired
- 1977-06-22 IE IE1277/77A patent/IE45151B1/en unknown
- 1977-06-22 SE SE7707245A patent/SE7707245A0/sv not_active Application Discontinuation
- 1977-06-22 NO NO772211A patent/NO148554B/no unknown
- 1977-06-23 HU HU77CI1752A patent/HU176501B/hu unknown
-
1982
- 1982-11-26 KE KE3247A patent/KE3247A/xx unknown
-
1984
- 1984-12-30 MY MY31/84A patent/MY8400031A/xx unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3196011A (en) | Electrostatic frosting | |
| US3147679A (en) | Electrostatic image transfer processes and apparatus therefor | |
| US5021318A (en) | Process for forming secure images | |
| US3542545A (en) | Frost or relief wrinkling of an imaging article comprising an electrically photosensitive layer and a deformable layer | |
| US3551146A (en) | Induction imaging system | |
| US4420244A (en) | Apparatus for developing latent electrostatic images for gap transfer to a carrier sheet | |
| US3238041A (en) | Relief imaging of photoresponsive member and product | |
| US3196008A (en) | Electrophotographic process for formation of frost-like deformation images in mechanically deformable photoconductive layers | |
| US3764311A (en) | Frost imaging system | |
| US5376491A (en) | Organic photoconductor | |
| US3335003A (en) | Reflex xerographic process | |
| US5965314A (en) | Intermediate transfer element for liquid electrophotography | |
| US3240596A (en) | Electrophotographic processes and apparatus | |
| US3975195A (en) | Migration imaging system | |
| NO123260B (US20020095090A1-20020718-M00002.png) | ||
| US3329500A (en) | Electrostatic frosting | |
| US3258336A (en) | Strippable layer frost printing | |
| US4101321A (en) | Imaging system | |
| NO148554B (no) | Analogifremgangsmaate til fremstilling av terapeutisk virksomme 1-(azacykliske aralkoksyfenyl)-2- eller -3-(bis-arylalkylamino)-alkaner | |
| US3458309A (en) | Color transparencies produced by electrophotographic techniques | |
| US3196765A (en) | Image development and projection | |
| US3677750A (en) | Photoelectrosolographic imaging process | |
| US3196010A (en) | Electrophotographic process for formation of deformation images in deformable interference films | |
| US5942360A (en) | Photoreceptor with low surface energy and process of making | |
| US3692404A (en) | Strippable layer relief printing |
