1,3-dipolární cykloadice (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "1,3-dipolární cykloadice" in Czech language version.

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36doi.org

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16acs.org

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9nih.gov

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3sciencedirect.com

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3wiley.com

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3web.archive.org

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2archive.today

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2harvard.edu

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2rsc.org

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2jst.go.jp

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2pnas.org

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1nature.com

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1heterocycles.jp

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1thieme-connect.com

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acs.org

pubs.acs.org

MLOSTON, G.; LANGHALS, E.; HUISGEN, Rolf. First Two-Step 1,2-Dipolar Cycloadditons: Nonstereospecificity. J. Am. Chem. Soc.. 1986, roč. 108, s. 6401–66402. Dostupné online. doi:10.1021/ja00280a053. (anglicky)
BERNER, Daniel; MCGARRITY, John. Direct observation of the methyldiazonium ion in fluorosulfuric acid. Journal of the American Chemical Society. 1979, roč. 101, s. 3135–3136. Dostupné online. doi:10.1021/ja00505a059. (anglicky)
HUISGEN, Rolf; SCHEER, Wolfgang; HUBER, Helmut. Stereospecific Conversion of cis-trans Isomeric Aziridines to Open-Chain Azomethine Ylides. Journal of the American Chemical Society. 1967, roč. 89, s. 1753–1755. Dostupné online. doi:10.1021/ja00983a052. (anglicky)
PADWA, Albert; SMOLANOFF, Joel. Photocycloaddition of arylazirenes with electron-deficient olefins. Journal of the American Chemical Society. 1971, roč. 93, s. 548–550. Dostupné online. doi:10.1021/ja00731a056. (anglicky)
BODE, Jeffrey; CARREIRA, Erick. Stereoselective Syntheses of Epothilones A and B via Directed Nitrile Oxide Cycloaddition.. Journal of the American Chemical Society. 2011, roč. 123, čís. 15, s. 3611–3612. Dostupné online. doi:10.1021/ja0155635. PMID 11472140. (anglicky)
CARAMELLA, Pierluigi; HOUK, K.N. Geometries of nitrilium betaines. The clarification of apparently anomalous reactions of 1,3-dipoles. Journal of the American Chemical Society. 1976, roč. 98, s. 6397–6399. Dostupné online. doi:10.1021/ja00436a062. (anglicky)
CARAMELLA, Pierluigi; GANDOUR, Ruth W.; HALL, Janet A.; DEVILLE, Cynthia G. A derivation of the shapes and energies of the molecular orbitals of 1,3-dipoles. Geometry optimizations of these species by MINDO/2 and MINDO/3. Journal of the American Chemical Society. 1977, roč. 99, s. 385–392. Dostupné online. doi:10.1021/ja00444a013. (anglicky)
EVANS, David; RIPIN, David; HALSTEAD, David; CAMPOS, Kevin. Synthesis and Absolute Stereochemical Assignment of (+)-Miyakolide. Journal of the American Chemical Society. 1999, roč. 121, s. 6816–6826. Dostupné online. doi:10.1021/ja990789h. (anglicky)
Padwa, A.; Hornbuckle, S. F. Ylide Formation from the Reaction of Carbenes and Carbenoids with Heteroatom Lone Pairs Chem Rev 1991, 91, 263.
Janulis, E. P.; Arduengo, A. J. Structure of an Electronically Stabilized Carbonyl Ylide J Am Chem Soc 1983, 105, 5929.
Prakash, G. K. S.; Ellis, R. W.; Felberg, J. D.; Olah, G. A. Formaldehyde 0-Methylide, [CH2=O+-CH2: The Parent Carbonyl Ylide] J Am Chem Soc 1986, 108, 1341.
Gisch, J. F.; Landgrebe, J. A. Dichlorocarbene from flash vacuum pyrolysis of trimethyl(trichloromethyl)silane. Possible observation of 1,1-dichloro-3-phenylcarbonyl ylide J Org Chem 1985, 50, 2050.
Huan, Z. W.; Landgrebe, J. A.; Peterson, K. Dibromocarbonyl ylides: Deoxygenation of aldehydes and ketones by dibromocarbene J Org Chem 1983, 48, 4519.
Martin, C. W.; Lund, P. R.; Rapp, E.; Landgrebe, J. A. Halogenated carbonyl ylides in the reactions of mercurial dihalocarbene precursors with substituted benzaldehydes J Org Chem 1978, 43, 1071.
Padwa, A.; Hertzog, D. L.; Nadler, W. R. Intramolecular Cycloaddition of Isomunchnone Dipoles to Heteroaromatic π-Systems J Org Chem 1994, 59, 7072.
ONISHI, Tomoyuki; SEBAHAR, Paul; WILLIAMS, Robert. Concise, Asymmetric Total Synthesis of Spirotryprostatin A. Organic Letters. 2003, roč. 5, s. 3135–3137. Dostupné online. doi:10.1021/ol0351910. PMID 12917000. (anglicky)

archive.org

FERNANDEZ-SUAREZ, Marta; BARUAH, Hemanta; MARTINEZ-HERNANDEZ, Laura; XIE, Kathleen. Redirecting lipoic acid ligase for cell surface protein labeling with small-molecule probes. Nature Biotechnology. 2007, roč. 25, s. 1483–1487. Dostupné online. doi:10.1038/nbt1355. PMID 18059260. (anglicky)

archive.today

HUISGEN, Rolf. Kinetics and Mechanism of 1,3-Dipolar Cycloadditions. Angewandte Chemie International Edition. November 1963, roč. 2, čís. 11, s. 633–645. Dostupné v archivu pořízeném dne 2012-12-11. doi:10.1002/anie.196306331. (anglicky)
HUISGEN, Rolf. Kinetics and Mechanism of 1,3-Dipolar Cycloadditions. Angewandte Chemie International Edition. November 1963, roč. 2, čís. 11, s. 633–645. Dostupné v archivu pořízeném dne 2012-12-11. doi:10.1002/anie.196306331. (anglicky)

doi.org

HUISGEN, Rolf. Kinetics and Mechanism of 1,3-Dipolar Cycloadditions. Angewandte Chemie International Edition. November 1963, roč. 2, čís. 11, s. 633–645. Dostupné v archivu pořízeném dne 2012-12-11. doi:10.1002/anie.196306331. (anglicky)
FIRESTONE, R. Mechanism of 1,3-dipolar cycloadditions. Journal of Organic Chemistry. 1968, roč. 33, s. 2285–2290. Dostupné online. doi:10.1021/jo01270a023. (anglicky)
HUISGEN, Rolf. 1,3-Dipolar cycloadditions. 76. Concerted nature of 1,3-dipolar cycloadditions and the question of diradical intermediates. Journal of Organic Chemistry. 1976, roč. 41, s. 403–419. Dostupné online. doi:10.1021/jo00865a001. (anglicky)
MLOSTON, G.; LANGHALS, E.; HUISGEN, Rolf. First Two-Step 1,2-Dipolar Cycloadditons: Nonstereospecificity. J. Am. Chem. Soc.. 1986, roč. 108, s. 6401–66402. Dostupné online. doi:10.1021/ja00280a053. (anglicky)
SEYYED AMIR, Siadati. An example of a stepwise mechanism for the catalyst-free 1,3-dipolar cycloaddition between a nitrile oxide and an electron rich alkene. Tetrahedron Letters. 2015, roč. 56, s. 4857–4863. Dostupné online. doi:10.1016/j.tetlet.2015.06.048. (anglicky)
HUISGEN, Rolf. 1,3-Dipolar Cycloadditions. Past and Future. Angewandte Chemie International Edition. 1963, roč. 2, s. 565–598. Dostupné online. doi:10.1002/anie.196305651. (anglicky)
COX, A; THOMAS, L; SHERIDAN, J. Microwave Spectra of Diazomethane and its Deutero Derivatives. Nature. 1958, roč. 181, čís. 4614, s. 1000–1001. Dostupné online. doi:10.1038/1811000a0. Bibcode 1958Natur.181.1000C. (anglicky)
HILBERTY, P; LEFORESTIER, C. Expansion of molecular orbital wave functions into valence bond wave functions. A simplified procedure.. Journal of the American Chemical Society. 1978, roč. 100, s. 2012–2017. Dostupné online. doi:10.1021/ja00475a007. (anglicky)
MCGARRITY, J.F.; PATAI, Saul. Basicity, acidity and hydrogen bonding. Diazonium and Diazo Groups. 1978, roč. 1, s. 179–230. Dostupné online. doi:10.1002/9780470771549.ch6. (anglicky)
BERNER, Daniel; MCGARRITY, John. Direct observation of the methyldiazonium ion in fluorosulfuric acid. Journal of the American Chemical Society. 1979, roč. 101, s. 3135–3136. Dostupné online. doi:10.1021/ja00505a059. (anglicky)
MULLER, Eugen; RUNDEL, Wolfgans. Untersuchungen an Diazomethanen, VI. Mitteil.: Umsetzung von Diazoäthan mit Methyllithium. Chemische Berichte. 1956, roč. 89, s. 1065–1071. Dostupné online. doi:10.1002/cber.19560890436. (anglicky)
BIHLMAIER, Werner; GEITTNER, Jochen; HUISGEN, Rolf; REISSIGP, Hans-Ulrich. The Stereospecificity of Diazomethane Cycloadditions. Heterocycles. 1978, roč. 10, s. 147–152. Dostupné online. doi:10.3987/S-1978-01-0147. (anglicky) Archivováno 11. 6. 2019 na Wayback Machine.
HUISGEN, Rolf; SCHEER, Wolfgang; HUBER, Helmut. Stereospecific Conversion of cis-trans Isomeric Aziridines to Open-Chain Azomethine Ylides. Journal of the American Chemical Society. 1967, roč. 89, s. 1753–1755. Dostupné online. doi:10.1021/ja00983a052. (anglicky)
DAHMEN, Alexander; HAMBERGER, Helmut; HUISGEN, Rolf; MARKOWSKI, Volker. Conrotatory ring opening of cyanostilbene oxides to carbonyl ylides. Journal of the Chemical Society D: Chemical Communications. 1971, čís. 19, s. 1192–1194. Dostupné online. doi:10.1039/C29710001192. (anglicky)
PADWA, Albert; SMOLANOFF, Joel. Photocycloaddition of arylazirenes with electron-deficient olefins. Journal of the American Chemical Society. 1971, roč. 93, s. 548–550. Dostupné online. doi:10.1021/ja00731a056. (anglicky)
IWASHITA, Takashi; KUSUMI, Takenori; KAKISAWA, Hiroshi. A Synthesis of dl-isoretronecanol. Chemistry Letters. 1979, čís. 11, s. 1337–1340. Dostupné online. doi:10.1246/cl.1979.1337. (anglicky) Archivováno 4. 7. 2018 na Wayback Machine.
WANG, Chia-Lin; RIPKA, William; CONFALONE, Pat. A short and stereospecific synthesis of (±)-α-lycorane. Tetrahedron Letters. 1984, roč. 25, s. 4613–4616. Dostupné online. doi:10.1016/S0040-4039(01)91213-4. (anglicky)
KANEMASA, Shuji. Metal-Assisted Stereocontrol of 1,3-Dipolar Cycloaddition Reactions. Synthesis Letters. 2002, roč. 2002, s. 1371–1387. Dostupné online. doi:10.1055/s-2002-33506. (anglicky)
BODE, Jeffrey; CARREIRA, Erick. Stereoselective Syntheses of Epothilones A and B via Directed Nitrile Oxide Cycloaddition.. Journal of the American Chemical Society. 2011, roč. 123, čís. 15, s. 3611–3612. Dostupné online. doi:10.1021/ja0155635. PMID 11472140. (anglicky)
Vsevolod V. Rostovtsev; Luke G. Green; Valery V. Fokin; K. Barry Sharpless. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective Ligation of Azides and Terminal Alkynes. Angewandte Chemie International Edition. 2002, roč. 41, čís. 14, s. 2596–22599. doi:10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4. PMID 12203546. (anglicky)
CARAMELLA, Pierluigi; HOUK, K.N. Geometries of nitrilium betaines. The clarification of apparently anomalous reactions of 1,3-dipoles. Journal of the American Chemical Society. 1976, roč. 98, s. 6397–6399. Dostupné online. doi:10.1021/ja00436a062. (anglicky)
CARAMELLA, Pierluigi; GANDOUR, Ruth W.; HALL, Janet A.; DEVILLE, Cynthia G. A derivation of the shapes and energies of the molecular orbitals of 1,3-dipoles. Geometry optimizations of these species by MINDO/2 and MINDO/3. Journal of the American Chemical Society. 1977, roč. 99, s. 385–392. Dostupné online. doi:10.1021/ja00444a013. (anglicky)
HUISGEN, Rolf. Kinetics and Mechanism of 1,3-Dipolar Cycloadditions. Angewandte Chemie International Edition. November 1963, roč. 2, čís. 11, s. 633–645. Dostupné v archivu pořízeném dne 2012-12-11. doi:10.1002/anie.196306331. (anglicky)
EVANS, David; RIPIN, David; HALSTEAD, David; CAMPOS, Kevin. Synthesis and Absolute Stereochemical Assignment of (+)-Miyakolide. Journal of the American Chemical Society. 1999, roč. 121, s. 6816–6826. Dostupné online. doi:10.1021/ja990789h. (anglicky)
ONISHI, Tomoyuki; SEBAHAR, Paul; WILLIAMS, Robert. Concise, Asymmetric Total Synthesis of Spirotryprostatin A. Organic Letters. 2003, roč. 5, s. 3135–3137. Dostupné online. doi:10.1021/ol0351910. PMID 12917000. (anglicky)
TORNOE, Christian; CHRISTENSEN, Caspar; MELDAL, Morten. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides. Journal of Organic Chemistry. 2002, roč. 67, čís. 9, s. 3057–3064. doi:10.1021/jo011148j. PMID 11975567. (anglicky)
ROSTOVTSEV, Vsevolod; GREEN, Luke; FOKIN, Valery; SHARPLESS, Barry K. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective Ligation of Azides and Terminal Alkynes. Angewandte Chemie International Edition. 2002, roč. 41, s. 2596–2599. doi:10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4. PMID 12203546. (anglicky)
BESANCENEY-WEBLER, Christen; JIANG, Hao; ZHENG, Tianqing; FENG, Lei. Increasing the Efficacy of Bioorthogonal Click Reactions for Bioconjugation: A Comparative Study. Angewandte Chemie International Edition. 2011, roč. 50, s. 8051–8056. Dostupné online. doi:10.1002/anie.201101817. PMID 21761519. (anglicky)
BREIDENBACH, Mark; GALLAGHER, Jennifer; KING, David; SMART, Brian. Targeted metabolic labeling of yeast N-glycans with unnatural sugars. Proceedings of the National Academy of Sciences of the United States of America. 2010, roč. 107, čís. 9, s. 3988–3993. Dostupné online. doi:10.1073/pnas.0911247107. PMID 20142501. Bibcode 2010PNAS..107.3988B. (anglicky)
AGARD, Nicholas; PRESCHER, Jennifer; BERTOZZI, Carolyn. A Strain-Promoted [3 + 2] Azide−Alkyne Cycloaddition for Covalent Modification of Biomolecules in Living Systems. Journal of the American Chemical Society. 2004, roč. 126, s. 15046–15047. doi:10.1021/ja044996f. PMID 15547999. (anglicky)
FERNANDEZ-SUAREZ, Marta; BARUAH, Hemanta; MARTINEZ-HERNANDEZ, Laura; XIE, Kathleen. Redirecting lipoic acid ligase for cell surface protein labeling with small-molecule probes. Nature Biotechnology. 2007, roč. 25, s. 1483–1487. Dostupné online. doi:10.1038/nbt1355. PMID 18059260. (anglicky)

dx.doi.org

HUISGEN, Rolf. 1.3-Dipolare Cycloadditionen Ruckschau und Ausblick.. Angewandte Chemie. 1963, roč. 75, s. 604–637. Dostupné online [abstract]. (anglicky)
FIRESTONE, R. Mechanism of 1,3-dipolar cycloadditions. Journal of Organic Chemistry. 1968, roč. 33, s. 2285–2290. Dostupné online. doi:10.1021/jo01270a023. (anglicky)
HUISGEN, Rolf. 1,3-Dipolar cycloadditions. 76. Concerted nature of 1,3-dipolar cycloadditions and the question of diradical intermediates. Journal of Organic Chemistry. 1976, roč. 41, s. 403–419. Dostupné online. doi:10.1021/jo00865a001. (anglicky)
HUISGEN, Rolf. 1,3-Dipolar Cycloadditions. Past and Future. Angewandte Chemie International Edition. 1963, roč. 2, s. 565–598. Dostupné online. doi:10.1002/anie.196305651. (anglicky)
HILBERTY, P; LEFORESTIER, C. Expansion of molecular orbital wave functions into valence bond wave functions. A simplified procedure.. Journal of the American Chemical Society. 1978, roč. 100, s. 2012–2017. Dostupné online. doi:10.1021/ja00475a007. (anglicky)

harvard.edu

adsabs.harvard.edu

COX, A; THOMAS, L; SHERIDAN, J. Microwave Spectra of Diazomethane and its Deutero Derivatives. Nature. 1958, roč. 181, čís. 4614, s. 1000–1001. Dostupné online. doi:10.1038/1811000a0. Bibcode 1958Natur.181.1000C. (anglicky)
BREIDENBACH, Mark; GALLAGHER, Jennifer; KING, David; SMART, Brian. Targeted metabolic labeling of yeast N-glycans with unnatural sugars. Proceedings of the National Academy of Sciences of the United States of America. 2010, roč. 107, čís. 9, s. 3988–3993. Dostupné online. doi:10.1073/pnas.0911247107. PMID 20142501. Bibcode 2010PNAS..107.3988B. (anglicky)

heterocycles.jp

BIHLMAIER, Werner; GEITTNER, Jochen; HUISGEN, Rolf; REISSIGP, Hans-Ulrich. The Stereospecificity of Diazomethane Cycloadditions. Heterocycles. 1978, roč. 10, s. 147–152. Dostupné online. doi:10.3987/S-1978-01-0147. (anglicky) Archivováno 11. 6. 2019 na Wayback Machine.

jst.go.jp

jstage.jst.go.jp

IWASHITA, Takashi; KUSUMI, Takenori; KAKISAWA, Hiroshi. A Synthesis of dl-isoretronecanol. Chemistry Letters. 1979, čís. 11, s. 1337–1340. Dostupné online. doi:10.1246/cl.1979.1337. (anglicky) Archivováno 4. 7. 2018 na Wayback Machine.
Hamaguchi, M.; Ibata, T. New Type of Mesoionic System. 1,3-Dipolar Cycloaddition of Isomunchnon With Ethylenic Compounds Archivováno 11. 4. 2020 na Wayback Machine. Chem Lett 1975, 499.

nature.com

COX, A; THOMAS, L; SHERIDAN, J. Microwave Spectra of Diazomethane and its Deutero Derivatives. Nature. 1958, roč. 181, čís. 4614, s. 1000–1001. Dostupné online. doi:10.1038/1811000a0. Bibcode 1958Natur.181.1000C. (anglicky)

nih.gov

ncbi.nlm.nih.gov

BODE, Jeffrey; CARREIRA, Erick. Stereoselective Syntheses of Epothilones A and B via Directed Nitrile Oxide Cycloaddition.. Journal of the American Chemical Society. 2011, roč. 123, čís. 15, s. 3611–3612. Dostupné online. doi:10.1021/ja0155635. PMID 11472140. (anglicky)
Vsevolod V. Rostovtsev; Luke G. Green; Valery V. Fokin; K. Barry Sharpless. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective Ligation of Azides and Terminal Alkynes. Angewandte Chemie International Edition. 2002, roč. 41, čís. 14, s. 2596–22599. doi:10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4. PMID 12203546. (anglicky)
ONISHI, Tomoyuki; SEBAHAR, Paul; WILLIAMS, Robert. Concise, Asymmetric Total Synthesis of Spirotryprostatin A. Organic Letters. 2003, roč. 5, s. 3135–3137. Dostupné online. doi:10.1021/ol0351910. PMID 12917000. (anglicky)
TORNOE, Christian; CHRISTENSEN, Caspar; MELDAL, Morten. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides. Journal of Organic Chemistry. 2002, roč. 67, čís. 9, s. 3057–3064. doi:10.1021/jo011148j. PMID 11975567. (anglicky)
ROSTOVTSEV, Vsevolod; GREEN, Luke; FOKIN, Valery; SHARPLESS, Barry K. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective Ligation of Azides and Terminal Alkynes. Angewandte Chemie International Edition. 2002, roč. 41, s. 2596–2599. doi:10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4. PMID 12203546. (anglicky)
BESANCENEY-WEBLER, Christen; JIANG, Hao; ZHENG, Tianqing; FENG, Lei. Increasing the Efficacy of Bioorthogonal Click Reactions for Bioconjugation: A Comparative Study. Angewandte Chemie International Edition. 2011, roč. 50, s. 8051–8056. Dostupné online. doi:10.1002/anie.201101817. PMID 21761519. (anglicky)
BREIDENBACH, Mark; GALLAGHER, Jennifer; KING, David; SMART, Brian. Targeted metabolic labeling of yeast N-glycans with unnatural sugars. Proceedings of the National Academy of Sciences of the United States of America. 2010, roč. 107, čís. 9, s. 3988–3993. Dostupné online. doi:10.1073/pnas.0911247107. PMID 20142501. Bibcode 2010PNAS..107.3988B. (anglicky)
AGARD, Nicholas; PRESCHER, Jennifer; BERTOZZI, Carolyn. A Strain-Promoted [3 + 2] Azide−Alkyne Cycloaddition for Covalent Modification of Biomolecules in Living Systems. Journal of the American Chemical Society. 2004, roč. 126, s. 15046–15047. doi:10.1021/ja044996f. PMID 15547999. (anglicky)
FERNANDEZ-SUAREZ, Marta; BARUAH, Hemanta; MARTINEZ-HERNANDEZ, Laura; XIE, Kathleen. Redirecting lipoic acid ligase for cell surface protein labeling with small-molecule probes. Nature Biotechnology. 2007, roč. 25, s. 1483–1487. Dostupné online. doi:10.1038/nbt1355. PMID 18059260. (anglicky)

pnas.org

Hodgson, D. M.; Bruckl, T.; Glen, R.; Labande, A. H.; Selden, D. A.; Dossetter, A. G.; Redgrave, A. J. Catalytic enantioselective intermolecular cycloadditions of 2-diazo-3,6-diketoester-derived carbonyl ylides with alkene dipolarophiles Proceedings of the National Academy of Sciences of the United States of America 2004, 101, 5450.
BREIDENBACH, Mark; GALLAGHER, Jennifer; KING, David; SMART, Brian. Targeted metabolic labeling of yeast N-glycans with unnatural sugars. Proceedings of the National Academy of Sciences of the United States of America. 2010, roč. 107, čís. 9, s. 3988–3993. Dostupné online. doi:10.1073/pnas.0911247107. PMID 20142501. Bibcode 2010PNAS..107.3988B. (anglicky)

rsc.org

pubs.rsc.org

DAHMEN, Alexander; HAMBERGER, Helmut; HUISGEN, Rolf; MARKOWSKI, Volker. Conrotatory ring opening of cyanostilbene oxides to carbonyl ylides. Journal of the Chemical Society D: Chemical Communications. 1971, čís. 19, s. 1192–1194. Dostupné online. doi:10.1039/C29710001192. (anglicky)
Sammes, P. G.; Street, L. J. Intra molecular Cyclo additions with Oxido pyrylium Ylides J. Chem. Soc., Chem. Commun. 1982, 1056.

sciencedirect.com

SEYYED AMIR, Siadati. An example of a stepwise mechanism for the catalyst-free 1,3-dipolar cycloaddition between a nitrile oxide and an electron rich alkene. Tetrahedron Letters. 2015, roč. 56, s. 4857–4863. Dostupné online. doi:10.1016/j.tetlet.2015.06.048. (anglicky)
WANG, Chia-Lin; RIPKA, William; CONFALONE, Pat. A short and stereospecific synthesis of (±)-α-lycorane. Tetrahedron Letters. 1984, roč. 25, s. 4613–4616. Dostupné online. doi:10.1016/S0040-4039(01)91213-4. (anglicky)
Garst, M. E.; McBride, B. J.; Douglass III, J. G. Intramolecular cycloadditions with 2-(ω-alkenyl)-5-hydroxy-4-pyrones Tetrahedron Lett. 1983, 24, 1675.

thieme-connect.com

KANEMASA, Shuji. Metal-Assisted Stereocontrol of 1,3-Dipolar Cycloaddition Reactions. Synthesis Letters. 2002, roč. 2002, s. 1371–1387. Dostupné online. doi:10.1055/s-2002-33506. (anglicky)

web.archive.org

BIHLMAIER, Werner; GEITTNER, Jochen; HUISGEN, Rolf; REISSIGP, Hans-Ulrich. The Stereospecificity of Diazomethane Cycloadditions. Heterocycles. 1978, roč. 10, s. 147–152. Dostupné online. doi:10.3987/S-1978-01-0147. (anglicky) Archivováno 11. 6. 2019 na Wayback Machine.
IWASHITA, Takashi; KUSUMI, Takenori; KAKISAWA, Hiroshi. A Synthesis of dl-isoretronecanol. Chemistry Letters. 1979, čís. 11, s. 1337–1340. Dostupné online. doi:10.1246/cl.1979.1337. (anglicky) Archivováno 4. 7. 2018 na Wayback Machine.
Hamaguchi, M.; Ibata, T. New Type of Mesoionic System. 1,3-Dipolar Cycloaddition of Isomunchnon With Ethylenic Compounds Archivováno 11. 4. 2020 na Wayback Machine. Chem Lett 1975, 499.

wiley.com

onlinelibrary.wiley.com

MCGARRITY, J.F.; PATAI, Saul. Basicity, acidity and hydrogen bonding. Diazonium and Diazo Groups. 1978, roč. 1, s. 179–230. Dostupné online. doi:10.1002/9780470771549.ch6. (anglicky)
MULLER, Eugen; RUNDEL, Wolfgans. Untersuchungen an Diazomethanen, VI. Mitteil.: Umsetzung von Diazoäthan mit Methyllithium. Chemische Berichte. 1956, roč. 89, s. 1065–1071. Dostupné online. doi:10.1002/cber.19560890436. (anglicky)
BESANCENEY-WEBLER, Christen; JIANG, Hao; ZHENG, Tianqing; FENG, Lei. Increasing the Efficacy of Bioorthogonal Click Reactions for Bioconjugation: A Comparative Study. Angewandte Chemie International Edition. 2011, roč. 50, s. 8051–8056. Dostupné online. doi:10.1002/anie.201101817. PMID 21761519. (anglicky)