Spiro compound (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Spiro compound" in English language version.

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14doi.org

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7nih.gov

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2worldcat.org

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2semanticscholar.org

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2qmul.ac.uk

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2books.google.com

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1harvard.edu

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1msu.edu

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1amazon.com

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1acdlabs.com

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acdlabs.com

"Spiro Hydrocarbons. Rule A-41. Compounds: Method 1".

amazon.com

Eliel, Ernest Ludwig; Wilen, Samuel H.; Mander, Lewis N. (1994). "Chirality in Molecules Devoid of Chiral Centers (Chapter 14)". Stereochemistry of Organic Compounds (1st ed.). New York, NY, USA: Wiley & Sons. pp. 1119–1190, esp. 1119ff, 1138ff, and passim. ISBN 978-0-471-01670-0. Retrieved 2 February 2016. For a further but less stable source of the same text that provides access to the relevant material, see [3], same access date.

books.google.com

Clayden, Jonathan; Greeves, Nick; Warren, Stuart (2012). Organic Chemistry (2nd ed.). Oxford, UK: Oxford University Press. pp. 319f, 432, 604, 653, 746, 803, 839, 846f. ISBN 978-0-19-927029-3. Retrieved 2 February 2016.
Eliel, Ernest Ludwig; Wilen, Samuel H.; Mander, Lewis N. (1994). "Chirality in Molecules Devoid of Chiral Centers (Chapter 14)". Stereochemistry of Organic Compounds (1st ed.). New York, NY, USA: Wiley & Sons. pp. 1119–1190, esp. 1119ff, 1138ff, and passim. ISBN 978-0-471-01670-0. Retrieved 2 February 2016. For a further but less stable source of the same text that provides access to the relevant material, see [3], same access date.

chemspider.com

"1,4-Dioxaspiro[4.5]decane". chemspider.com. Retrieved 3 February 2016.

doi.org

De Meijere, Armin; von Seebach, Malte; Zöllner, Stefan; Kozhushkov, Sergei I.; Belov, Vladimir N.; Boese, Roland; Haumann, Thomas; Benet-Buchholz, Jordi; Yufit, Dmitrii S.; Howard, Judith A. K. (2001). "Spirocyclopropanated Bicyclopropylidenes: Straightforward Preparation, Physical Properties, and Chemical Transformations". Chemistry - A European Journal. 7 (18): 4021–4034. doi:10.1002/1521-3765(20010917)7:18<4021::AID-CHEM4021>3.0.CO;2-E. PMID 11596945.
Moss, G.P. (1999). "Extension and Revision of the Nomenclature for Spiro Compounds". Pure Appl. Chem. 71 (3): 531–558. doi:10.1351/pac199971030531. ISSN 1365-3075. S2CID 20131819. Note, the article co-authors, the Working Party of the IUPAC (1992-1998), were P. M. Giles, Jr., E. W. Godly, K.-H. Hellwich, A. K. Ikizler, M. V. Kisakürek, A. D. McNaught, G. P. Moss, J. Nyitrai, W. H. Powell, O. Weissbach, and A. Yerin. Also available online at "Extension and Revision of the Nomenclature for Spiro Compounds". London, GBR: Queen Mary University of London. Retrieved 3 February 2016. Also available in German, with et al. indicating the same working party, at Hellwich, Karl-Heinz; et al. (18 October 2002). "Erweiterung und Revision der Nomenklatur der Spiroverbindungen". Angewandte Chemie. 114 (20): 4073–4089. Bibcode:2002AngCh.114.4073H. doi:10.1002/1521-3757(20021018)114:20<4073::AID-ANGE4073>3.0.CO;2-T. Die Übersetzung basiert auf der "Extension and Revision of the Nomenclature for Spiro Compounds" der Commission on Nomenclature of Organic Chemistry (III.1) der Organic Chemistry Division der International Union of Pure and Applied Chemistry, veröffentlicht in Pure Appl. Chem. 1999, 71, 531–558.
Smith, Laura K. & Baxendale, Ian R. (2015). "Total Syntheses of Natural Products Containing Spirocarbocycles". Org. Biomol. Chem. 13 (39): 9907–9933. doi:10.1039/C5OB01524C. PMID 26356301.
Dixon, Joseph A.; Naro, Paul A. (1960). "Syntheses of Four Spiro Hydrocarbons". The Journal of Organic Chemistry. 25 (12): 2094–2097. doi:10.1021/jo01082a006.
Nakamura, Masaharu; Wang, Xiao Qun; Isaka, Masahiko; Yamago, Shigeru; Nakamura, Eiichi (2003). "Synthesis and [3+2] Cycloaddition of a 2,2-Dialkoxy-1-methylenecyclopropane: 6,6-Dimethyl-1-methylene-4,8-Dioxaspiro[2.5]octane and cis-5-(5,5-Dimethyl-1,3-dioxan-2-ylidene)hexahydro-1(2H)-pentalen-2-one". Organic Syntheses. 80: 144. doi:10.15227/orgsyn.080.0144.
Wender, Paul A.; White, Alan W.; McDonald, Frank E. (1992). "Spiroannelation Via Organobis(Cuprates): 9,9-Dimethylspiro[4.5]Decan-7-One". Organic Syntheses. 70: 204. doi:10.15227/orgsyn.070.0204.
Bartolo, Nicole D.; Robson, Ryan N.; Witt, Collin H.; Woerpel, K. A. (2024). "Preparation of a Radical Clocks Bearing Carbonyl Groups: Synthesis of N-Methoxy-N-methylspiro[cyclopropane-1,9'-fluorene]-2-carboxamide". Organic Syntheses. 101: 61–80. doi:10.15227/orgsyn.101.0061.
Viatcheslav Stepanenko, Kun Huang, Margarita Ortiz-Marciales (2010). "Synthesis of Spiroborate Esters from 1,2-Aminoalcohols, Ethylene Glycol and Triisopropyl Borate: Preparation of (S)-1-(1,3,2-Dioxaborolan-2-Yloxy)-3-Methyl-1,1-Diphenylbutan-2-Amine". Organic Syntheses. 87: 26. doi:10.15227/orgsyn.087.0026. PMC 2915795.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Craig, Robert; Smith, R. C.; Pritchett, B. P.; Estipona, B. I.; Stoltz, B. M. (2016). "Preparation of 1,5-Dioxaspiro[5.5]undecan-3-one". Organic Syntheses. 93: 210–227. doi:10.15227/orgsyn.093.0210. PMC 5514842. PMID 28729749.
"Stereocontrolled Preparation of 3-Acyltetrahydrofurans from Acid-Promoted Rearrangements of Allylic Ketals: (2S,3S)-3-Acetyl-8-Carboethoxy-2,3-Dimethyl-1-Oxa-8-Azaspiro[4.5]Decane". Organic Syntheses. 71: 63. 1993. doi:10.15227/orgsyn.071.0063.
"Dichlorovinylation of an Enolate: 8-Ethynyl-8-Methyl-1,4-Dioxaspiro[4.5]Dec-6-Ene". Organic Syntheses. 64: 73. 1986. doi:10.15227/orgsyn.064.0073.
Rios, Ramon (2012). "Enantioselective Methodologies for the Synthesis of Spiro Compounds". Chemical Society Reviews. 41 (3): 1060–1074. doi:10.1039/C1CS15156H. PMID 21975423.
von Baeyer, Adolf (1900). "Systematik und Nomenclatur Bicyclischer Kohlenwasserstoffe". Berichte der Deutschen Chemischen Gesellschaft. 33 (3): 3771–3775. doi:10.1002/cber.190003303187.
Moss, G.P. (1999). "Extension and Revision of the Nomenclature for Spiro Compounds". Pure Appl. Chem. 71 (3): 531–558. doi:10.1351/pac199971030531. ISSN 1365-3075. S2CID 20131819. The full author (Working Party) list and a link to a German translation are provided in a corresponding footnote. Also available online at "Extension and Revision of the Nomenclature for Spiro Compounds". London, GBR: Queen Mary University of London.

harvard.edu

ui.adsabs.harvard.edu

Moss, G.P. (1999). "Extension and Revision of the Nomenclature for Spiro Compounds". Pure Appl. Chem. 71 (3): 531–558. doi:10.1351/pac199971030531. ISSN 1365-3075. S2CID 20131819. Note, the article co-authors, the Working Party of the IUPAC (1992-1998), were P. M. Giles, Jr., E. W. Godly, K.-H. Hellwich, A. K. Ikizler, M. V. Kisakürek, A. D. McNaught, G. P. Moss, J. Nyitrai, W. H. Powell, O. Weissbach, and A. Yerin. Also available online at "Extension and Revision of the Nomenclature for Spiro Compounds". London, GBR: Queen Mary University of London. Retrieved 3 February 2016. Also available in German, with et al. indicating the same working party, at Hellwich, Karl-Heinz; et al. (18 October 2002). "Erweiterung und Revision der Nomenklatur der Spiroverbindungen". Angewandte Chemie. 114 (20): 4073–4089. Bibcode:2002AngCh.114.4073H. doi:10.1002/1521-3757(20021018)114:20<4073::AID-ANGE4073>3.0.CO;2-T. Die Übersetzung basiert auf der "Extension and Revision of the Nomenclature for Spiro Compounds" der Commission on Nomenclature of Organic Chemistry (III.1) der Organic Chemistry Division der International Union of Pure and Applied Chemistry, veröffentlicht in Pure Appl. Chem. 1999, 71, 531–558.

msu.edu

www2.chemistry.msu.edu

For all four categories, see Reusch, William (1999). "Saturated Hydrocarbons, Alkanes and Cycloalkanes: Cycloalkanes (Table: Examples of Isomeric C₈H₁₄ Bicycloalkanes) or Nomenclature: Cycloalkanes (same Table), and passim". Virtual Text of Organic Chemistry (Jan. 2016 ed.). East Lansing, MI, USA: Michigan State University, Department of Chemistry. Retrieved 3 February 2016. The specific chapters can be found at [1] and [2], respectively, same access date. For the description featuring adjacent atoms for all but the isolated category, see Clayden, op. cit.

nih.gov

pubmed.ncbi.nlm.nih.gov

De Meijere, Armin; von Seebach, Malte; Zöllner, Stefan; Kozhushkov, Sergei I.; Belov, Vladimir N.; Boese, Roland; Haumann, Thomas; Benet-Buchholz, Jordi; Yufit, Dmitrii S.; Howard, Judith A. K. (2001). "Spirocyclopropanated Bicyclopropylidenes: Straightforward Preparation, Physical Properties, and Chemical Transformations". Chemistry - A European Journal. 7 (18): 4021–4034. doi:10.1002/1521-3765(20010917)7:18<4021::AID-CHEM4021>3.0.CO;2-E. PMID 11596945.
Smith, Laura K. & Baxendale, Ian R. (2015). "Total Syntheses of Natural Products Containing Spirocarbocycles". Org. Biomol. Chem. 13 (39): 9907–9933. doi:10.1039/C5OB01524C. PMID 26356301.
Craig, Robert; Smith, R. C.; Pritchett, B. P.; Estipona, B. I.; Stoltz, B. M. (2016). "Preparation of 1,5-Dioxaspiro[5.5]undecan-3-one". Organic Syntheses. 93: 210–227. doi:10.15227/orgsyn.093.0210. PMC 5514842. PMID 28729749.
Rios, Ramon (2012). "Enantioselective Methodologies for the Synthesis of Spiro Compounds". Chemical Society Reviews. 41 (3): 1060–1074. doi:10.1039/C1CS15156H. PMID 21975423.

ncbi.nlm.nih.gov

Viatcheslav Stepanenko, Kun Huang, Margarita Ortiz-Marciales (2010). "Synthesis of Spiroborate Esters from 1,2-Aminoalcohols, Ethylene Glycol and Triisopropyl Borate: Preparation of (S)-1-(1,3,2-Dioxaborolan-2-Yloxy)-3-Methyl-1,1-Diphenylbutan-2-Amine". Organic Syntheses. 87: 26. doi:10.15227/orgsyn.087.0026. PMC 2915795.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Craig, Robert; Smith, R. C.; Pritchett, B. P.; Estipona, B. I.; Stoltz, B. M. (2016). "Preparation of 1,5-Dioxaspiro[5.5]undecan-3-one". Organic Syntheses. 93: 210–227. doi:10.15227/orgsyn.093.0210. PMC 5514842. PMID 28729749.

pubchem.ncbi.nlm.nih.gov

Pubchem. "1,1'-Bicyclopentyl-1,1'-diol". nih.gov. Retrieved 7 March 2016.

qmul.ac.uk

chem.qmul.ac.uk

Moss, G.P. (1999). "Extension and Revision of the Nomenclature for Spiro Compounds". Pure Appl. Chem. 71 (3): 531–558. doi:10.1351/pac199971030531. ISSN 1365-3075. S2CID 20131819. Note, the article co-authors, the Working Party of the IUPAC (1992-1998), were P. M. Giles, Jr., E. W. Godly, K.-H. Hellwich, A. K. Ikizler, M. V. Kisakürek, A. D. McNaught, G. P. Moss, J. Nyitrai, W. H. Powell, O. Weissbach, and A. Yerin. Also available online at "Extension and Revision of the Nomenclature for Spiro Compounds". London, GBR: Queen Mary University of London. Retrieved 3 February 2016. Also available in German, with et al. indicating the same working party, at Hellwich, Karl-Heinz; et al. (18 October 2002). "Erweiterung und Revision der Nomenklatur der Spiroverbindungen". Angewandte Chemie. 114 (20): 4073–4089. Bibcode:2002AngCh.114.4073H. doi:10.1002/1521-3757(20021018)114:20<4073::AID-ANGE4073>3.0.CO;2-T. Die Übersetzung basiert auf der "Extension and Revision of the Nomenclature for Spiro Compounds" der Commission on Nomenclature of Organic Chemistry (III.1) der Organic Chemistry Division der International Union of Pure and Applied Chemistry, veröffentlicht in Pure Appl. Chem. 1999, 71, 531–558.
Moss, G.P. (1999). "Extension and Revision of the Nomenclature for Spiro Compounds". Pure Appl. Chem. 71 (3): 531–558. doi:10.1351/pac199971030531. ISSN 1365-3075. S2CID 20131819. The full author (Working Party) list and a link to a German translation are provided in a corresponding footnote. Also available online at "Extension and Revision of the Nomenclature for Spiro Compounds". London, GBR: Queen Mary University of London.

semanticscholar.org

api.semanticscholar.org

Moss, G.P. (1999). "Extension and Revision of the Nomenclature for Spiro Compounds". Pure Appl. Chem. 71 (3): 531–558. doi:10.1351/pac199971030531. ISSN 1365-3075. S2CID 20131819. Note, the article co-authors, the Working Party of the IUPAC (1992-1998), were P. M. Giles, Jr., E. W. Godly, K.-H. Hellwich, A. K. Ikizler, M. V. Kisakürek, A. D. McNaught, G. P. Moss, J. Nyitrai, W. H. Powell, O. Weissbach, and A. Yerin. Also available online at "Extension and Revision of the Nomenclature for Spiro Compounds". London, GBR: Queen Mary University of London. Retrieved 3 February 2016. Also available in German, with et al. indicating the same working party, at Hellwich, Karl-Heinz; et al. (18 October 2002). "Erweiterung und Revision der Nomenklatur der Spiroverbindungen". Angewandte Chemie. 114 (20): 4073–4089. Bibcode:2002AngCh.114.4073H. doi:10.1002/1521-3757(20021018)114:20<4073::AID-ANGE4073>3.0.CO;2-T. Die Übersetzung basiert auf der "Extension and Revision of the Nomenclature for Spiro Compounds" der Commission on Nomenclature of Organic Chemistry (III.1) der Organic Chemistry Division der International Union of Pure and Applied Chemistry, veröffentlicht in Pure Appl. Chem. 1999, 71, 531–558.
Moss, G.P. (1999). "Extension and Revision of the Nomenclature for Spiro Compounds". Pure Appl. Chem. 71 (3): 531–558. doi:10.1351/pac199971030531. ISSN 1365-3075. S2CID 20131819. The full author (Working Party) list and a link to a German translation are provided in a corresponding footnote. Also available online at "Extension and Revision of the Nomenclature for Spiro Compounds". London, GBR: Queen Mary University of London.

thefreelibrary.com

"Elusive bowtie pinned down". The Free Library. 13 July 1991. Retrieved 2 February 2016.

tufts.edu

perseus.tufts.edu

Lewis, Charlton T. (1890). "spīra [dictionary entry]". An Elementary Latin Dictionary. New York, NY, USA: American Book Company. Retrieved 3 February 2016. Quoting: 'spīra ae, f, σπεῖρα, a coil, fold, twist, spiral: in spirain se conligit anguis, V., O.: longo iactetur spira galero, i. e. tie, Iu.' The Greek transcription, σπεῖρα, reflects the use of this cognate as one ancient Greek term to refer to a coil or related fold, see Woodhouse, S.C. (1910). "Fold, subs. [dictionary entry]". English-Greek Dictionary: A Vocabulary of the Attic Language. Ludgate Hill [London, ENG]: George Routledge & Sons. Retrieved 3 February 2016. Quoting: 'Fold, subs. … Coil : V. σπεῖρα… see coil.'

uchicago.edu

artflsrv02.uchicago.edu

Lewis, Charlton T. (1890). "spīra [dictionary entry]". An Elementary Latin Dictionary. New York, NY, USA: American Book Company. Retrieved 3 February 2016. Quoting: 'spīra ae, f, σπεῖρα, a coil, fold, twist, spiral: in spirain se conligit anguis, V., O.: longo iactetur spira galero, i. e. tie, Iu.' The Greek transcription, σπεῖρα, reflects the use of this cognate as one ancient Greek term to refer to a coil or related fold, see Woodhouse, S.C. (1910). "Fold, subs. [dictionary entry]". English-Greek Dictionary: A Vocabulary of the Attic Language. Ludgate Hill [London, ENG]: George Routledge & Sons. Retrieved 3 February 2016. Quoting: 'Fold, subs. … Coil : V. σπεῖρα… see coil.'

worldcat.org

search.worldcat.org

Moss, G.P. (1999). "Extension and Revision of the Nomenclature for Spiro Compounds". Pure Appl. Chem. 71 (3): 531–558. doi:10.1351/pac199971030531. ISSN 1365-3075. S2CID 20131819. Note, the article co-authors, the Working Party of the IUPAC (1992-1998), were P. M. Giles, Jr., E. W. Godly, K.-H. Hellwich, A. K. Ikizler, M. V. Kisakürek, A. D. McNaught, G. P. Moss, J. Nyitrai, W. H. Powell, O. Weissbach, and A. Yerin. Also available online at "Extension and Revision of the Nomenclature for Spiro Compounds". London, GBR: Queen Mary University of London. Retrieved 3 February 2016. Also available in German, with et al. indicating the same working party, at Hellwich, Karl-Heinz; et al. (18 October 2002). "Erweiterung und Revision der Nomenklatur der Spiroverbindungen". Angewandte Chemie. 114 (20): 4073–4089. Bibcode:2002AngCh.114.4073H. doi:10.1002/1521-3757(20021018)114:20<4073::AID-ANGE4073>3.0.CO;2-T. Die Übersetzung basiert auf der "Extension and Revision of the Nomenclature for Spiro Compounds" der Commission on Nomenclature of Organic Chemistry (III.1) der Organic Chemistry Division der International Union of Pure and Applied Chemistry, veröffentlicht in Pure Appl. Chem. 1999, 71, 531–558.
Moss, G.P. (1999). "Extension and Revision of the Nomenclature for Spiro Compounds". Pure Appl. Chem. 71 (3): 531–558. doi:10.1351/pac199971030531. ISSN 1365-3075. S2CID 20131819. The full author (Working Party) list and a link to a German translation are provided in a corresponding footnote. Also available online at "Extension and Revision of the Nomenclature for Spiro Compounds". London, GBR: Queen Mary University of London.

zenodo.org

von Baeyer, Adolf (1900). "Systematik und Nomenclatur Bicyclischer Kohlenwasserstoffe". Berichte der Deutschen Chemischen Gesellschaft. 33 (3): 3771–3775. doi:10.1002/cber.190003303187.