171d91a5e60072479ecbdd4dc82cb417 intjou_a2019v20n18.pdf 13362e1bb573d1ed8ee0b7fc65bd779e561e593c intjou_a2019v20n18.pdf 2a59a9c71cde8853c97749088d05aae787eba6fc6fe5bde7dcb7089fa5b29b19 intjou_a2019v20n18.pdf Producer: iText® 7.1.1 ©2000-2018 iText Group NV (AGPL-version) CreationDate: Fri Sep 6 12:06:05 2019 CEST ModDate: Fri Sep 6 12:06:05 2019 CEST Tagged: no UserProperties: no Suspects: no Form: none JavaScript: no Pages: 13 Encrypted: no Page size: 595.276 x 841.89 pts (A4) Page rot: 0 File size: 1165922 bytes Optimized: no PDF version: 1.7 name type encoding emb sub uni object ID ------------------------------------ ----------------- ---------------- --- --- --- --------- OSZGOO+URWPalladioL-Ital Type 1 Custom yes yes no 10 0 CSFEPQ+URWPalladioL-Bold Type 1 Custom yes yes no 15 0 LZDGTK+Rpxb Type 1 Builtin yes yes no 19 0 RJXJLW+URWPalladioL-Roma Type 1 Custom yes yes no 23 0 SVVJCD+Rpxr Type 1 Builtin yes yes no 27 0 FSCNAL+EURM10 Type 1 Builtin yes yes no 31 0 WLENKM+VnURWPalladioL-Bold Type 1 Custom yes yes no 35 0 DRYAID+VnURWPalladioL Type 1 Custom yes yes no 40 0 IRWHZX+TimesNewRomanPSMT Type 1C WinAnsi yes yes no 48 0 CKUPDE+TimesNewRomanPS-BoldItalicMT Type 1C WinAnsi yes yes no 51 0 MCBCCI+SourceSansRoman-Regular Type 1C Custom yes yes no 68 0 MCBCCM+SourceSansRoman.613wght Type 1C Custom yes yes no 72 0 MCBCCO+SourceSansRoman-Bold Type 1C Custom yes yes no 76 0 JNLIIF+Rpxi Type 1 Builtin yes yes no 90 0 UPQBDO+Pxsy Type 1 Builtin yes yes no 94 0 TGMEOR+Rpcxr Type 1 Builtin yes yes no 112 0 Jhove (Rel. 1.6, 2011-01-04) Date: 2019-11-06 05:12:12 CET RepresentationInformation: intjou_a2019v20n18.pdf ReportingModule: PDF-hul, Rel. 1.8 (2009-05-22) LastModified: 2019-10-03 10:34:23 CEST Size: 1165922 Format: PDF Version: 1.7 Status: Well-Formed and valid SignatureMatches: PDF-hul MIMEtype: application/pdf PDFMetadata: Objects: 300 FreeObjects: 1 IncrementalUpdates: 0 DocumentCatalog: PageLayout: SinglePage PageMode: UseNone Outlines: Item: Title: Introduction Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@6a6824be Item: Title: Results and Discussion Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@5c8da962 Children: Item: Title: Amphiphiles from 1,2-Disubstituted Cyclobutane Scaffolds: Surfactants and LMWG Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@512ddf17 Item: Title: Highly Rigid Polydentate Ligands From 1,3-disubstituted Cyclobutane Scaffolds Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@2c13da15 Item: Title: Materials and Methods Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@77556fd Children: Item: Title: General Procedures Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@368239c8 Item: Title: Experimental Section Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@9e89d68 Children: Item: Title: Synthesis of tert-Butyl (1S,2R)-2-Hydroxymethylcyclobutane-1-Carboxylate (2) Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@3b192d32 Item: Title: Synthesis of tert-Butyl (1R,2S)-2-Tosyloxymethylcyclobutane-1-Carboxylate (3) Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@16f65612 Item: Title: Synthesis of tert-Butyl (1S,2R)-2-Dodecanamidomethylcyclobutane-1-Carboxylate (5) through amine 4 Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@311d617d Item: Title: Synthesis of (1S,2R)-2-Dodecanamidomethylcyclobutane-1-Carboxylic Acid (6) Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@7c53a9eb Item: Title: Synthesis of tert-Butyl (1S,2R)-2-Hydroxymethylcyclobutane-1-Carbamate (8) Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@ed17bee Item: Title: Synthesis of (1S,2R)-1-tert-Butyloxycarbonylaminocyclobutane-1-Methyl Dodecanoate (11) Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@2a33fae0 Item: Title: Synthesis of (1S,2R)-2-Dodecanoyloxymethylcyclobutane-1-Ammonium Chloride (12) Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@707f7052 Item: Title: Synthesis of tert-Butyl (1S,2R)-2-Tosyloxymethylcyclobutane-1-Carboxylate (9) Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@11028347 Item: Title: Synthesis of tert-Butyl (1S,2S)-2-Dodecanamidomethylcyclobutane-1-Carbamate (13) through diamine 10 Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@14899482 Item: Title: Synthesis of (1S,2R)-2-Dodecanamidomethylcyclobutane-1-Ammonium Chloride (14) Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@21588809 Item: Title: Synthesis of Diamides 16 and 17. General Procedure Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@2aae9190 Item: Title: Synthesis of Tetra-tert-Butyl N,N,N’,N’-[((1S,3R)-2,2-Dimethylcyclobutane-1,3-diyl) Bis(Methylene)Bis(Azanetriyl)] Tetraacetate (20) Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@2f333739 Item: Title: Synthesis of N,N,N’,N’-[((1S,3R)-2,2-dimethylcyclobutane-1,3-diyl) bis(methylene)-bis(azanetriyl)] tetraacetic acid (21) Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@77468bd9 Item: Title: Synthesis of Dimethyl 6,6'-[{2,2-Dimethylcyclobutane-1,3-diylbis[(2-tert-butoxy-2-oxoethyl)- azanemethylenediyl]}bis(methylene)] dipicolinate (24) through compound (23) Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@12bb4df8 Item: Title: Synthesis of 6,6'-[{2,2-dimethylcyclobutane-1,3-diylbis[(carboxymethyl) azane methylene diyl]}- bis(methylene)] dipicolinic acid (25) Destination: 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