Allenes - sources analisys of the English Wikipedia aritle

Analisys of sources in references of the Wikipedia ariticle en.wikipedia.org/wiki/Allenes

Site	Hosts in references	Count	Global rank	English rank
doi.org	doi.org↓ (65), dx.doi.org↓ (1)	66	54	180
acs.org	pubs.acs.org↓ (16)	16	925	1020
rsc.org	xlink.rsc.org↓ (5), pubs.rsc.org↓ (3)	8	1487	1531
worldcat.org	worldcat.org↓ (6)	6	68	276
wiley.com	onlinelibrary.wiley.com↓ (4), doi.wiley.com↓ (2)	6	202	476
elsevier.com	linkinghub.elsevier.com↓ (5)	5	718	1313
orgsyn.org	orgsyn.org↓ (4)	4	4169	9497
semanticscholar.org	api.semanticscholar.org↓ (4)	4	228	140
nist.gov	webbook.nist.gov↓ (1)	1	177	252
books.google.com	books.google.com↓ (1)	1	1	1
harvard.edu	ui.adsabs.harvard.edu↓ (1)	1	121	134
degruyter.com	degruyter.com↓ (1)	1	2376	2706
iupac.org	goldbook.iupac.org↓ (1)	1	284	889
springer.com	link.springer.com↓ (1)	1	290	528
thieme-connect.de	thieme-connect.de↓ (1)	1	low	low
actachemscand.org	actachemscand.org↓ (1)	1	low	low
qmul.ac.uk	chem.qmul.ac.uk↓ (1)	1	1711	2313

actachemscand.org

49. Skattebøl, Lars; Nilsson, Martin; Lindberg, Bengt; McKay, James; Munch-Petersen, Jon (1963). "The Synthesis of Allenes from 1,1-Dihalocyclopropane Derivatives and Alkyllithium". Acta Chemica Scandinavica. 17: 1683–1693. doi:10.3891/acta.chem.scand.17-1683. ISSN 0904-213X.

api.semanticscholar.org

9. Maitland, Peter; Mills, W. H. (1935). "Experimental Demonstration of the Allene Asymmetry". Nature. 135 (3424): 994. Bibcode:1935Natur.135Q.994M. doi:10.1038/135994a0. S2CID 4085600.
41. Pinho e Melo, Teresa M. V. D. (July 2011). "Allenes as building blocks in heterocyclic chemistry". Monatshefte für Chemie - Chemical Monthly. 142 (7): 681–697. doi:10.1007/s00706-011-0505-7. ISSN 0026-9247. S2CID 189843060.
64. Ma, Shengming (2006-01-01). "Transition-metal-catalyzed reactions of allenes". Pure and Applied Chemistry. 78 (2): 197–208. doi:10.1351/pac200678020197. ISSN 1365-3075. S2CID 97529095.
72. "Nomenclature for cyclic organic compounds with contiguous formal double bonds (the δ-convention)". Pure Appl. Chem. 60: 1395-1401. 1988. doi:10.1351/pac198860091395. S2CID 97759274.

books.google.com

8. Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 978-0-471-72091-1

chem.qmul.ac.uk

72. "Nomenclature for cyclic organic compounds with contiguous formal double bonds (the δ-convention)". Pure Appl. Chem. 60: 1395-1401. 1988. doi:10.1351/pac198860091395. S2CID 97759274.

degruyter.com

64. Ma, Shengming (2006-01-01). "Transition-metal-catalyzed reactions of allenes". Pure and Applied Chemistry. 78 (2): 197–208. doi:10.1351/pac200678020197. ISSN 1365-3075. S2CID 97529095.

doi.org

1. IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "allenes". doi:10.1351/goldbook.A00238
3. Taylor, David R. (1967-06-01). "The Chemistry of Allenes". Chemical Reviews. 67 (3): 317–359. doi:10.1021/cr60247a004. ISSN 0009-2665.
4. Hoffmann-Röder, Anja; Krause, Norbert (2004-02-27). "Synthesis and Properties of Allenic Natural Products and Pharmaceuticals". Angewandte Chemie International Edition. 43 (10): 1196–1216. doi:10.1002/anie.200300628. ISSN 1433-7851. PMID 14991780.
5. Burton, B. S.; von Pechmann, H. (January 1887). "Ueber die Einwirkung von Chlorphosphor auf Acetondicarbonsäureäther". Berichte der Deutschen Chemischen Gesellschaft (in German). 20 (1): 145–149. doi:10.1002/cber.18870200136.
6. Jones, E. R. H.; Mansfield, G. H.; Whiting, M. C. (1954). "Researches on acetylenic compounds. Part XLVII. The prototropic rearrangements of some acetylenic dicarboxylic acids". Journal of the Chemical Society (Resumed): 3208–3212. doi:10.1039/jr9540003208. ISSN 0368-1769.
9. Maitland, Peter; Mills, W. H. (1935). "Experimental Demonstration of the Allene Asymmetry". Nature. 135 (3424): 994. Bibcode:1935Natur.135Q.994M. doi:10.1038/135994a0. S2CID 4085600.
10. Rivera Fuentes, Pablo; Diederich, François (2012). "Allenes in Molecular Materials". Angew. Chem. Int. Ed. Engl. 51 (12): 2818–2828. doi:10.1002/anie.201108001. PMID 22308109.
11. Celmer, Walter D.; Solomons, I. A. (1952). "The Structure of the Antibiotic Mycomycin". Journal of the American Chemical Society. 74 (7): 1870–1871. doi:10.1021/ja01127a529. ISSN 0002-7863.
13. H. Hendon, Christopher; Tiana, Davide; T. Murray, Alexander; R. Carbery, David; Walsh, Aron (2013). "Helical frontier orbitals of conjugated linear molecules". Chemical Science. 4 (11): 4278–4284. doi:10.1039/C3SC52061G.
13. H. Hendon, Christopher; Tiana, Davide; T. Murray, Alexander; R. Carbery, David; Walsh, Aron (2013). "Helical frontier orbitals of conjugated linear molecules". Chemical Science. 4 (11): 4278–4284. doi:10.1039/C3SC52061G.
14. Garner, Marc H.; Hoffmann, Roald; Rettrup, Sten; Solomon, Gemma C. (2018-06-27). "Coarctate and Möbius: The Helical Orbitals of Allene and Other Cumulenes". ACS Central Science. 4 (6): 688–700. doi:10.1021/acscentsci.8b00086. ISSN 2374-7943. PMC 6026781. PMID 29974064.
15. Informatics, NIST Office of Data and (1997). "Welcome to the NIST WebBook". webbook.nist.gov. doi:10.18434/T4D303. Retrieved 2020-10-17.
16. Alabugin, Igor V. (2016-09-19). Stereoelectronic Effects: A Bridge Between Structure and Reactivity. Chichester, UK: John Wiley & Sons, Ltd. doi:10.1002/9781118906378. ISBN 978-1-118-90637-8.
18. Alcaide, Benito; Almendros, Pedro; Aragoncillo, Cristina (2010-01-28). "Exploiting [2+2] cycloaddition chemistry: achievements with allenes". Chemical Society Reviews. 39 (2): 783–816. doi:10.1039/B913749A. hdl:10261/29537. ISSN 1460-4744. PMID 20111793.
19. Pasto, Daniel J. (January 1984). "Recent developments in allene chemistry". Tetrahedron. 40 (15): 2805–2827. doi:10.1016/S0040-4020(01)91289-X.
20. Alcaide, Benito; Almendros, Pedro (August 2004). "The Allenic Pauson−Khand Reaction in Synthesis". European Journal of Organic Chemistry. 2004 (16): 3377–3383. doi:10.1002/ejoc.200400023. ISSN 1434-193X.
21. Mascareñas, José L.; Varela, Iván; López, Fernando (2019-02-19). "Allenes and Derivatives in Gold(I)- and Platinum(II)-Catalyzed Formal Cycloadditions". Accounts of Chemical Research. 52 (2): 465–479. doi:10.1021/acs.accounts.8b00567. ISSN 0001-4842. PMC 6497370. PMID 30640446.
22. Zi, Weiwei; Toste, F. Dean (2016-08-08). "Recent advances in enantioselective gold catalysis". Chemical Society Reviews. 45 (16): 4567–4589. doi:10.1039/C5CS00929D. ISSN 1460-4744. PMID 26890605.
23. Lee, Mitchell; Nguyen, Mary; Brandt, Chance; Kaminsky, Werner; Lalic, Gojko (2017-12-04). "Catalytic Hydroalkylation of Allenes". Angewandte Chemie International Edition. 56 (49): 15703–15707. doi:10.1002/anie.201709144. PMID 29052303.
23. Lee, Mitchell; Nguyen, Mary; Brandt, Chance; Kaminsky, Werner; Lalic, Gojko (2017-12-04). "Catalytic Hydroalkylation of Allenes". Angewandte Chemie International Edition. 56 (49): 15703–15707. doi:10.1002/anie.201709144. PMID 29052303.
24. Kim, Seung Wook; Meyer, Cole C.; Mai, Binh Khanh; Liu, Peng; Krische, Michael J. (2019-10-04). "Inversion of Enantioselectivity in Allene Gas versus Allyl Acetate Reductive Aldehyde Allylation Guided by Metal-Centered Stereogenicity: An Experimental and Computational Study". ACS Catalysis. 9 (10): 9158–9163. doi:10.1021/acscatal.9b03695. PMC 6921087. PMID 31857913.
25. Robinson, Marin S.; Polak, Mark L.; Bierbaum, Veronica M.; DePuy, Charles H.; Lineberger, W. C. (1995-06-01). "Experimental Studies of Allene, Methylacetylene, and the Propargyl Radical: Bond Dissociation Energies, Gas-Phase Acidities, and Ion-Molecule Chemistry". Journal of the American Chemical Society. 117 (25): 6766–6778. doi:10.1021/ja00130a017. ISSN 0002-7863.
25. Robinson, Marin S.; Polak, Mark L.; Bierbaum, Veronica M.; DePuy, Charles H.; Lineberger, W. C. (1995-06-01). "Experimental Studies of Allene, Methylacetylene, and the Propargyl Radical: Bond Dissociation Energies, Gas-Phase Acidities, and Ion-Molecule Chemistry". Journal of the American Chemical Society. 117 (25): 6766–6778. doi:10.1021/ja00130a017. ISSN 0002-7863.
26. Jones, E. R. H.; Mansfield, G. H.; Whiting, M. C. (1954-01-01). "Researches on acetylenic compounds. Part XLVII. The prototropic rearrangements of some acetylenic dicarboxylic acids". Journal of the Chemical Society (Resumed): 3208–3212. doi:10.1039/JR9540003208. ISSN 0368-1769.
27. Crabbé, Pierre; Nassim, Bahman; Robert-Lopes, Maria-Teresa. "One-Step Homologation of Acetylenes to Allenes: 4-Hydroxynona-1,2-diene [1,2-Nonadien-4-ol]". Organic Syntheses. 63: 203. doi:10.15227/orgsyn.063.0203.; Collective Volume, vol. 7, p. 276
28. Luo, Hongwen; Ma, Dengke; Ma, Shengming (2017). "Buta-2,3-dien-1-ol". Organic Syntheses: 153–166. doi:10.15227/orgsyn.094.0153.
29. Yoshikai, Naohiko; Nakamura, Eiichi (2012-04-11). "Mechanisms of Nucleophilic Organocopper(I) Reactions". Chemical Reviews. 112 (4): 2339–2372. doi:10.1021/cr200241f. ISSN 0009-2665. PMID 22111574.
30. Cripps, H. N.; Kiefer, E. F. "Allene". Organic Syntheses. 42: 12. doi:10.15227/orgsyn.042.0012.; Collective Volume, vol. 5, p. 22
31. Lang, Robert W.; Hansen, Hans-Jürgen (1980). "Eine einfache Allencarbonsäureester-Synthese mittels der Wittig-Reaktion" [A simple synthesis of allene carboxylic acid esters by means of the Wittig reaction]. Helv. Chim. Acta. 63 (2): 438–455. doi:10.1002/hlca.19800630215.
32. Lang, Robert W.; Hansen, Hans-Jürgen. "α-Allenic Esters from α-Phosphoranylidene Esters and Acid Chlorides: Ethyl 2,3-Pentadienoate [2,3-Pentadienoic acid, ethyl ester]". Organic Syntheses. 62: 202. doi:10.15227/orgsyn.062.0202.; Collective Volume, vol. 7, p. 232
33. Michelot, Didier; Clinet, Jean-Claude; Linstrumelle, Gérard (1982-01-01). "Allenyllithium Reagents (VI)1. A Highly Regioselective Metalation of Allenic Hydrocarbons2. A Route to Mono, DI, TRI or Tetrasubstituted Allenes". Synthetic Communications. 12 (10): 739–747. doi:10.1080/00397918208061912. ISSN 0039-7911.
33. Michelot, Didier; Clinet, Jean-Claude; Linstrumelle, Gérard (1982-01-01). "Allenyllithium Reagents (VI)1. A Highly Regioselective Metalation of Allenic Hydrocarbons2. A Route to Mono, DI, TRI or Tetrasubstituted Allenes". Synthetic Communications. 12 (10): 739–747. doi:10.1080/00397918208061912. ISSN 0039-7911.
37. Pasto, Daniel J. (January 1984). "Recent developments in allene chemistry". Tetrahedron. 40 (15): 2805–2827. doi:10.1016/S0040-4020(01)91289-X.
38. Zimmer, Reinhold; Dinesh, Chimmanamada U.; Nandanan, Erathodiyil; Khan, Faiz Ahmed (2000-08-01). "Palladium-Catalyzed Reactions of Allenes". Chemical Reviews. 100 (8): 3067–3126. doi:10.1021/cr9902796. ISSN 0009-2665. PMID 11749314.
39. Ma, Shengming (2009-10-20). "Electrophilic Addition and Cyclization Reactions of Allenes". Accounts of Chemical Research. 42 (10): 1679–1688. doi:10.1021/ar900153r. ISSN 0001-4842. PMID 19603781.
40. Alcaide, Benito; Almendros, Pedro; Aragoncillo, Cristina (2010). "Exploiting [2+2] cycloaddition chemistry: achievements with allenes". Chem. Soc. Rev. 39 (2): 783–816. doi:10.1039/B913749A. ISSN 0306-0012. PMID 20111793.
41. Pinho e Melo, Teresa M. V. D. (July 2011). "Allenes as building blocks in heterocyclic chemistry". Monatshefte für Chemie - Chemical Monthly. 142 (7): 681–697. doi:10.1007/s00706-011-0505-7. ISSN 0026-9247. S2CID 189843060.
42. López, Fernando; Mascareñas, José Luis (2011-01-10). "Allenes as Three‐Carbon Units in Catalytic Cycloadditions: New Opportunities with Transition‐Metal Catalysts". Chemistry – A European Journal. 17 (2): 418–428. doi:10.1002/chem.201002366. ISSN 0947-6539. PMID 21207554.
43. Aubert, Corinne; Fensterbank, Louis; Garcia, Pierre; Malacria, Max; Simonneau, Antoine (2011-03-09). "Transition Metal Catalyzed Cycloisomerizations of 1, n -Allenynes and -Allenenes". Chemical Reviews. 111 (3): 1954–1993. doi:10.1021/cr100376w. ISSN 0009-2665. PMID 21391568.
44. Krause, Norbert; Winter, Christian (2011-03-09). "Gold-Catalyzed Nucleophilic Cyclization of Functionalized Allenes: A Powerful Access to Carbo- and Heterocycles". Chemical Reviews. 111 (3): 1994–2009. doi:10.1021/cr1004088. ISSN 0009-2665. PMID 21314182.
45. Sydnes, Leiv K. (2003-04-01). "Allenes from Cyclopropanes and Their Use in Organic SynthesisRecent Developments". Chemical Reviews. 103 (4): 1133–1150. doi:10.1021/cr010025w. ISSN 0009-2665. PMID 12683779.
46. Brummond, Kay; DeForrest, Jolie (March 2007). "Synthesizing Allenes Today (1982-2006)". Synthesis. 2007 (6): 795–818. doi:10.1055/s-2007-965963. ISSN 0039-7881.
47. Yu, Shichao; Ma, Shengming (2011). "How easy are the syntheses of allenes?". Chemical Communications. 47 (19): 5384–5418. doi:10.1039/C0CC05640E. ISSN 1359-7345. PMID 21409186.
48. Tejedor, David; Méndez-Abt, Gabriela; Cotos, Leandro; García-Tellado, Fernando (2013). "Propargyl Claisen rearrangement: allene synthesis and beyond". Chem. Soc. Rev. 42 (2): 458–471. doi:10.1039/C2CS35311C. ISSN 0306-0012. PMID 23034723.
49. Skattebøl, Lars; Nilsson, Martin; Lindberg, Bengt; McKay, James; Munch-Petersen, Jon (1963). "The Synthesis of Allenes from 1,1-Dihalocyclopropane Derivatives and Alkyllithium". Acta Chemica Scandinavica. 17: 1683–1693. doi:10.3891/acta.chem.scand.17-1683. ISSN 0904-213X.
50. Moore, William R.; Ward, Harold R. (December 1962). "The Formation of Allenes from gem-Dihalocyclopropanes by Reaction with Alkyllithium Reagents 1,2". The Journal of Organic Chemistry. 27 (12): 4179–4181. doi:10.1021/jo01059a013. ISSN 0022-3263.
51. Fedoryński, Michał (2003-04-01). "Syntheses of gem -Dihalocyclopropanes and Their Use in Organic Synthesis". Chemical Reviews. 103 (4): 1099–1132. doi:10.1021/cr0100087. ISSN 0009-2665. PMID 12683778.
53. Shi, Min; Shao, Li-Xiong; Lu, Jian-Mei; Wei, Yin; Mizuno, Kazuhiko; Maeda, Hajime (2010-10-13). "Chemistry of Vinylidenecyclopropanes". Chemical Reviews. 110 (10): 5883–5913. doi:10.1021/cr900381k. ISSN 0009-2665. PMID 20518460.
54. Ireland, Robert E.; Mueller, Richard H.; Willard, Alvin K. (May 1976). "The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation". Journal of the American Chemical Society. 98 (10): 2868–2877. doi:10.1021/ja00426a033. ISSN 0002-7863.
55. Kurtz, Kimberly C.M.; Frederick, Michael O.; Lambeth, Robert H.; Mulder, Jason A.; Tracey, Michael R.; Hsung, Richard P. (April 2006). "Synthesis of chiral allenes from ynamides through a highly stereoselective Saucy–Marbet rearrangement". Tetrahedron. 62 (16): 3928–3938. doi:10.1016/j.tet.2005.11.087.
56. Mukai, Chisato; Kobayashi, Minoru; Kubota, Shoko; Takahashi, Yukie; Kitagaki, Shinji (March 2004). "Construction of Azacycles Based on Endo-Mode Cyclization of Allenes". The Journal of Organic Chemistry. 69 (6): 2128–2136. doi:10.1021/jo035729f. ISSN 0022-3263. PMID 15058962.
57. Mukai, Chisato; Ohta, Masaru; Yamashita, Haruhisa; Kitagaki, Shinji (October 2004). "Base-Catalyzed Endo-Mode Cyclization of Allenes: Easy Preparation of Five- to Nine-Membered Oxacycles". The Journal of Organic Chemistry. 69 (20): 6867–6873. doi:10.1021/jo0488614. ISSN 0022-3263. PMID 15387613.
58. Pasto, Daniel J. (January 1984). "Recent developments in allene chemistry". Tetrahedron. 40 (15): 2805–2827. doi:10.1016/S0040-4020(01)91289-X.
59. Ma, Shengming (2009-10-20). "Electrophilic Addition and Cyclization Reactions of Allenes". Accounts of Chemical Research. 42 (10): 1679–1688. doi:10.1021/ar900153r. ISSN 0001-4842. PMID 19603781.
60. Yu, Shichao; Ma, Shengming (2012-03-26). "Allenes in Catalytic Asymmetric Synthesis and Natural Product Syntheses". Angewandte Chemie International Edition. 51 (13): 3074–3112. doi:10.1002/anie.201101460. PMID 22271630.
61. Ma, Shengming (2005-07-01). "Some Typical Advances in the Synthetic Applications of Allenes". Chemical Reviews. 105 (7): 2829–2872. doi:10.1021/cr020024j. ISSN 0009-2665. PMID 16011326.
64. Ma, Shengming (2006-01-01). "Transition-metal-catalyzed reactions of allenes". Pure and Applied Chemistry. 78 (2): 197–208. doi:10.1351/pac200678020197. ISSN 1365-3075. S2CID 97529095.
65. Bates, Roderick W.; Satcharoen, Vachiraporn (2002-03-06). "Nucleophilic transition metal based cyclization of allenes". Chemical Society Reviews. 31 (1): 12–21. doi:10.1039/b103904k. PMID 12108979.
66. Cherney, Emily C.; Green, Jason C.; Baran, Phil S. (2013-08-19). "Synthesis of ent -Kaurane and Beyerane Diterpenoids by Controlled Fragmentations of Overbred Intermediates". Angewandte Chemie International Edition. 52 (34): 9019–9022. doi:10.1002/anie.201304609. PMC 3814173. PMID 23861294.
67. Wiesner, K. (August 1975). "On the stereochemistry of photoaddition between α,β-unsaturated ketones and olefins". Tetrahedron. 31 (15): 1655–1658. doi:10.1016/0040-4020(75)85082-4.
68. Rahman, W.; Kuivila, Henry G. (March 1966). "Synthesis of Some Alkylidenecyclopropanes from Allenes 1". The Journal of Organic Chemistry. 31 (3): 772–776. doi:10.1021/jo01341a029. ISSN 0022-3263.
69. Krause, Norbert; Hoffmann‐Röder, Anja (2004). "18. Allenic Natural Products and Pharmaceuticals". In Krause, Norbert; Hashmi, A. Stephen K. (eds.). Modern Allene Chemistry. pp. 997–1040. doi:10.1002/9783527619573.ch18. ISBN 9783527619573.
70. Otsuka, Sei; Nakamura, Akira "Acetylene and allene complexes: their implication in homogeneous catalysis" Advances in Organometallic Chemistry 1976, volume 14, pp. 245-83. doi:10.1016/S0065-3055(08)60654-1.
71. Bhagwat, M. M.; Devaprabhakara, D. (1972). "Selective hydrogenation of allenes with chlorotris-(triphenylphosphine) rhodium catalyst". Tetrahedron Letters. 13 (15): 1391–1392. doi:10.1016/S0040-4039(01)84636-0.
72. "Nomenclature for cyclic organic compounds with contiguous formal double bonds (the δ-convention)". Pure Appl. Chem. 60: 1395-1401. 1988. doi:10.1351/pac198860091395. S2CID 97759274.

doi.wiley.com

16. Alabugin, Igor V. (2016-09-19). Stereoelectronic Effects: A Bridge Between Structure and Reactivity. Chichester, UK: John Wiley & Sons, Ltd. doi:10.1002/9781118906378. ISBN 978-1-118-90637-8.
20. Alcaide, Benito; Almendros, Pedro (August 2004). "The Allenic Pauson−Khand Reaction in Synthesis". European Journal of Organic Chemistry. 2004 (16): 3377–3383. doi:10.1002/ejoc.200400023. ISSN 1434-193X.

dx.doi.org

11. Celmer, Walter D.; Solomons, I. A. (1952). "The Structure of the Antibiotic Mycomycin". Journal of the American Chemical Society. 74 (7): 1870–1871. doi:10.1021/ja01127a529. ISSN 0002-7863.

goldbook.iupac.org

1. IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "allenes". doi:10.1351/goldbook.A00238

link.springer.com

41. Pinho e Melo, Teresa M. V. D. (July 2011). "Allenes as building blocks in heterocyclic chemistry". Monatshefte für Chemie - Chemical Monthly. 142 (7): 681–697. doi:10.1007/s00706-011-0505-7. ISSN 0026-9247. S2CID 189843060.

linkinghub.elsevier.com

19. Pasto, Daniel J. (January 1984). "Recent developments in allene chemistry". Tetrahedron. 40 (15): 2805–2827. doi:10.1016/S0040-4020(01)91289-X.
37. Pasto, Daniel J. (January 1984). "Recent developments in allene chemistry". Tetrahedron. 40 (15): 2805–2827. doi:10.1016/S0040-4020(01)91289-X.
55. Kurtz, Kimberly C.M.; Frederick, Michael O.; Lambeth, Robert H.; Mulder, Jason A.; Tracey, Michael R.; Hsung, Richard P. (April 2006). "Synthesis of chiral allenes from ynamides through a highly stereoselective Saucy–Marbet rearrangement". Tetrahedron. 62 (16): 3928–3938. doi:10.1016/j.tet.2005.11.087.
58. Pasto, Daniel J. (January 1984). "Recent developments in allene chemistry". Tetrahedron. 40 (15): 2805–2827. doi:10.1016/S0040-4020(01)91289-X.
67. Wiesner, K. (August 1975). "On the stereochemistry of photoaddition between α,β-unsaturated ketones and olefins". Tetrahedron. 31 (15): 1655–1658. doi:10.1016/0040-4020(75)85082-4.

onlinelibrary.wiley.com

4. Hoffmann-Röder, Anja; Krause, Norbert (2004-02-27). "Synthesis and Properties of Allenic Natural Products and Pharmaceuticals". Angewandte Chemie International Edition. 43 (10): 1196–1216. doi:10.1002/anie.200300628. ISSN 1433-7851. PMID 14991780.
5. Burton, B. S.; von Pechmann, H. (January 1887). "Ueber die Einwirkung von Chlorphosphor auf Acetondicarbonsäureäther". Berichte der Deutschen Chemischen Gesellschaft (in German). 20 (1): 145–149. doi:10.1002/cber.18870200136.
42. López, Fernando; Mascareñas, José Luis (2011-01-10). "Allenes as Three‐Carbon Units in Catalytic Cycloadditions: New Opportunities with Transition‐Metal Catalysts". Chemistry – A European Journal. 17 (2): 418–428. doi:10.1002/chem.201002366. ISSN 0947-6539. PMID 21207554.
60. Yu, Shichao; Ma, Shengming (2012-03-26). "Allenes in Catalytic Asymmetric Synthesis and Natural Product Syntheses". Angewandte Chemie International Edition. 51 (13): 3074–3112. doi:10.1002/anie.201101460. PMID 22271630.

orgsyn.org

27. Crabbé, Pierre; Nassim, Bahman; Robert-Lopes, Maria-Teresa. "One-Step Homologation of Acetylenes to Allenes: 4-Hydroxynona-1,2-diene [1,2-Nonadien-4-ol]". Organic Syntheses. 63: 203. doi:10.15227/orgsyn.063.0203.; Collective Volume, vol. 7, p. 276
28. Luo, Hongwen; Ma, Dengke; Ma, Shengming (2017). "Buta-2,3-dien-1-ol". Organic Syntheses: 153–166. doi:10.15227/orgsyn.094.0153.
30. Cripps, H. N.; Kiefer, E. F. "Allene". Organic Syntheses. 42: 12. doi:10.15227/orgsyn.042.0012.; Collective Volume, vol. 5, p. 22
32. Lang, Robert W.; Hansen, Hans-Jürgen. "α-Allenic Esters from α-Phosphoranylidene Esters and Acid Chlorides: Ethyl 2,3-Pentadienoate [2,3-Pentadienoic acid, ethyl ester]". Organic Syntheses. 62: 202. doi:10.15227/orgsyn.062.0202.; Collective Volume, vol. 7, p. 232

pubs.acs.org

3. Taylor, David R. (1967-06-01). "The Chemistry of Allenes". Chemical Reviews. 67 (3): 317–359. doi:10.1021/cr60247a004. ISSN 0009-2665.
29. Yoshikai, Naohiko; Nakamura, Eiichi (2012-04-11). "Mechanisms of Nucleophilic Organocopper(I) Reactions". Chemical Reviews. 112 (4): 2339–2372. doi:10.1021/cr200241f. ISSN 0009-2665. PMID 22111574.
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