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Propellane (English Wikipedia)

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

refsWebsite
Global rank English rank
35doi.org
2nd place
2nd place
10nih.gov
4th place
4th place
1semanticscholar.org
11th place
8th place
1harvard.edu
18th place
17th place

doi.org (Global: 2nd place; English: 2nd place)

  • Dilmaç, A. M.; Spuling, E.; de Meijere, A.; Bräse, S. (2017). "Propellanes—From a Chemical Curiosity to "Explosive" Materials and Natural Products". Angew. Chem. Int. Ed. 56 (21): 5684–5718. doi:10.1002/anie.201603951. PMID 27905166.
  • Osmont; et al. (2008). "Physicochemical Properties and Thermochemistry of Propellanes". Energy and Fuels. 22 (4): 2241–2257. doi:10.1021/ef8000423.
  • Altman, J.; Babad, E.; Itzchaki, J.; Ginsburg, D. (1966). "Propellanes—I". Tetrahedron. 22: 279–304. doi:10.1016/S0040-4020(01)82189-X.
  • Wiberg, Kenneth B. (1986). "The Concept of Strain in Organic Chemistry". Angew. Chem. Int. Ed. Engl. 25 (4): 312–322. doi:10.1002/anie.198603121.
  • Michl, Josef; Radziszewski, George J.; Downing, John W.; Wiberg, Kenneth B.; Walker, Frederick H.; Miller, Robert D.; Kovacic, Peter; Jawdosiuk, Mikolaj; Bonačić-Koutecký, Vlasta (1983). "Highly strained single and double bonds". Pure Appl. Chem. 55 (2): 315–321. doi:10.1351/pac198855020315.
  • Shaik, Sason; Danovich, David; Wu, Wei; Hiberty, Philippe C. (2009). "Charge-shift bonding and its manifestations in chemistry". Nature Chemistry. 1 (6): 443–449. doi:10.1038/nchem.327. PMID 21378912.
  • Sterling, Alistair J.; Dürr, Alexander B.; Smith, Russel C.; Anderson, Edward A.; Duarte, Fernanda (2020). "Rationalizing the diverse reactivity of [1.1.1]propellane through σ–π-delocalization". Chem. Sci. 11 (19): 4895–4903. doi:10.1039/D0SC01386B. PMC 8159217. PMID 34122945.
  • Wiberg, Kenneth B.; Waddell, Sherman T. (1990). "Reactions of [1.1.1]propellane". J. Am. Chem. Soc. 112 (6): 2194–2216. doi:10.1021/ja00162a022.
  • Fuchs, Josef; Szeimies, Günter (1992). "Synthese von [n.1.1]Propellanen (n = 2, 3, 4)". Chem. Ber. 125 (11): 2517–2522. doi:10.1002/cber.19921251126.
  • Frank, Nils; Nugent, Jeremy; Shire, Bethany R.; Pickford, Helena D.; Rabe, Patrick; Sterling, Alistair J.; Zarganes-Tzitzikas, Tryfon; Grimes, Thomas; Thompson, Amber L.; Smith, Russell C.; Schofield, Christopher J.; Brennan, Paul E.; Duarte, Fernanda; Anderson, Edward A. (2022). "Synthesis of meta-substituted arene bioisosteres from [3.1.1]propellane". Nature. 611 (7937): 721–726. doi:10.1038/s41586-022-05290-z. PMID 36108675. S2CID 252310498.
  • Kaszynski, Piotr; Michl, Josef (1988). "[n]Staffanes: a molecular-size "Tinkertoy" construction set for nanotechnology. Preparation of end-functionalized telomers and a polymer of [1.1.1]propellane". J. Am. Chem. Soc. 110 (15): 5225–5226. doi:10.1021/ja00223a070.
  • Wiberg, Kenneth B.; Burgmaier, George J. (1972). "Tricyclo[3.2.1.01,5]octane. A 3,2,1-Propellane". J. Am. Chem. Soc. 94 (21): 7396–7401. doi:10.1021/ja00776a022.
  • Weber, Robert W.; Cook, James M. (1978). "General method for the synthesis of [n.3.3]propellanes, n ≥ 3". Can. J. Chem. 56 (2): 189–192. doi:10.1139/v78-030.
  • Wiberg, Kenneth B.; Walker, Frederick H. (1982). "[1.1.1]Propellane". J. Am. Chem. Soc. 104 (19): 5239–5240. doi:10.1021/ja00383a046.
  • Stepan, Antonia F.; et al. (2012). "Application of the Bicyclo[1.1.1]pentane Motif as a Nonclassical Phenyl Ring Bioisostere in the Design of a Potent and Orally Active γ-Secretase Inhibitor". J. Med. Chem. 55 (7): 3414–3424. doi:10.1021/jm300094u. PMID 22420884.
  • Jarosch, Oliver; Szeimies, Günter (2003). "Thermal Behavior of [2.1.1]Propellane: A DFT/Ab Initio Study". J. Org. Chem. 68 (10): 3797–3801. doi:10.1021/jo020741d. PMID 12737556.
  • Walker, Frederick H.; Wiberg, Kenneth B.; Michl, Josef (1982). "[2.2.1]Propellane". J. Am. Chem. Soc. 104 (7): 2056. doi:10.1021/ja00371a059.
  • Gassman, P. G.; Proehl, G. S. (1980). "[3.1.1]Propellane". J. Am. Chem. Soc. 102 (22): 6862. doi:10.1021/ja00542a040.
  • Wiberg, Kenneth B.; Burgmaier, George J. (1969). "Tricyclo[3.2.1.01,5]octane". Tetrahedron Letters. 10 (5): 317–319. doi:10.1016/s0040-4039(01)87681-4.
  • Gassman, Paul G.; Topp, Alwin; Keller, John W. (1969). "Tricyclo[3.2.1.01,5]octane – a highly strained "propellerane"". Tetrahedron Letters. 10 (14): 1093–1095. doi:10.1016/s0040-4039(01)97748-2.
  • Aue, D. H.; Reynolds, R. N. (1974). "Reactions of a highly strained propellane. Tetracyclo[4.2.1.12,5.O1,6]decane". J. Org. Chem. 39 (15): 2315. doi:10.1021/jo00929a051.
  • Wiberg, Kenneth B.; Pratt, William E.; Bailey, William F. (1977). "Reaction of 1,4-diiodonorbornane, 1,4-diiodobicyclo[2.2.2]octane, and 1,5-diiodobicyclo[3.2.1]octane with butyllithium. Convenient preparative routes to the [2.2.2]- and [3.2.1]propellanes". J. Am. Chem. Soc. 99 (7): 2297–2302. doi:10.1021/ja00449a045.
  • Hamon, David P. G.; Trenerry, V. Craige (1981). "Carbenoid insertion reactions: formation of [4.1.1]propellane". J. Am. Chem. Soc. 103 (16): 4962–4965. doi:10.1021/ja00406a059.
  • Szeimies-Seebach, Ursula; Harnish, J.; Szeimies, Günter; Meerssche, M. V.; Germain, G.; Declerq, J. P. (1978). "Existence of a New C6H6 Isomer: Tricyclo[3.1.0.02,6]hex-1(6)-ene". Angew. Chem. Int. Ed. Engl. 17 (11): 848. doi:10.1002/anie.197808481.
  • Szeimies-Seebach, Ursula; Szeimies, Günter (1978). "A facile route to the [4.1.1]propellane system". J. Am. Chem. Soc. 100 (12): 3966–3967. doi:10.1021/ja00480a072.
  • Eaton, Philip E.; Temme, George H. (1973). "[2.2.2]Propellane system". J. Am. Chem. Soc. 95 (22): 7508–7510. doi:10.1021/ja00803a052.
  • Yang, S.; Cook, James M. (1976). "Reactions of dicarbonyl compounds with dimethyl β-ketoglutarate: II. Simple synthesis of compounds of the [10.3.3]- and [6.3.3]-propellane series". J. Org. Chem. 41 (11): 1903–1907. doi:10.1021/jo00873a004.
  • Pincock, Richard E.; Torupka, Edward J. (1969). "Tetracyclo[3.3.1.13,7.01,3]decane. Highly reactive 1,3-dehydro derivative of adamantane". J. Am. Chem. Soc. 91 (16): 4593. doi:10.1021/ja01044a072.
  • Mlinaric-Majerski, K.; Majerski, Z. (1980). "2,4-Methano-2,4-dehydroadamantane. A [3.1.1]propellane". J. Am. Chem. Soc. 102 (4): 1418. doi:10.1021/ja00524a033.
  • Tian, X; Li, L; Hu, Y; Zhang, H; Liu, Y; Chen, H; Ding, G; Zou, Z (2013). "Dichrocephones A and B, two cytotoxic sesquiterpenoids with the unique [3.3.3] propellane nucleus skeleton from Dichrocephala benthamii". RSC Adv. 3 (19): 7880–7883. Bibcode:2013RSCAd...3.7880T. doi:10.1039/C3RA23364B.
  • Schmiedel, V. M.; Hong, Y. J.; Lentz, D; Tantillo, D. J.; Christmann, M (2018). "Synthesis and Structure Revision of Dichrocephones A and B". Angew. Chem. Int. Ed. 57 (9): 2419–2422. doi:10.1002/anie.201711766. PMID 29251825.
  • Schneider, L. M.; Schmiedel, V. M.; Pecchioli, T; Lentz, T; Merten, C; Christmann, M (2017). "Asymmetric Synthesis of Carbocyclic Propellanes". Org. Lett. 19 (9): 2310–2313. doi:10.1021/acs.orglett.7b00836. PMID 28445060.
  • Dougherty, D.; Bloomfield, J. J.; Newkome, G. R.; Arnett, J. F.; McGlynn, S. P. (1976). "Photoelectron spectra of carbonyls. Propellenes and propellanones". The Journal of Physical Chemistry. 80 (20): 2212–2219. doi:10.1021/j100561a017.
  • Davidson, Ernest R. (1997). "Could 2.2.2-Propellatriene Exist?". Journal of the American Chemical Society. 119 (6): 1449. doi:10.1021/ja963652p.
  • Yang, Jian-Xiong; Wang, Yan Alexander (2021). "How Long Can a C–C σ-Single Bond Be?". The Journal of Physical Chemistry A. 125 (4): 933–942. doi:10.1021/acs.jpca.0c08924. PMID 33474940.

harvard.edu (Global: 18th place; English: 17th place)

ui.adsabs.harvard.edu

  • Tian, X; Li, L; Hu, Y; Zhang, H; Liu, Y; Chen, H; Ding, G; Zou, Z (2013). "Dichrocephones A and B, two cytotoxic sesquiterpenoids with the unique [3.3.3] propellane nucleus skeleton from Dichrocephala benthamii". RSC Adv. 3 (19): 7880–7883. Bibcode:2013RSCAd...3.7880T. doi:10.1039/C3RA23364B.

nih.gov (Global: 4th place; English: 4th place)

pubmed.ncbi.nlm.nih.gov

  • Dilmaç, A. M.; Spuling, E.; de Meijere, A.; Bräse, S. (2017). "Propellanes—From a Chemical Curiosity to "Explosive" Materials and Natural Products". Angew. Chem. Int. Ed. 56 (21): 5684–5718. doi:10.1002/anie.201603951. PMID 27905166.
  • Shaik, Sason; Danovich, David; Wu, Wei; Hiberty, Philippe C. (2009). "Charge-shift bonding and its manifestations in chemistry". Nature Chemistry. 1 (6): 443–449. doi:10.1038/nchem.327. PMID 21378912.
  • Sterling, Alistair J.; Dürr, Alexander B.; Smith, Russel C.; Anderson, Edward A.; Duarte, Fernanda (2020). "Rationalizing the diverse reactivity of [1.1.1]propellane through σ–π-delocalization". Chem. Sci. 11 (19): 4895–4903. doi:10.1039/D0SC01386B. PMC 8159217. PMID 34122945.
  • Frank, Nils; Nugent, Jeremy; Shire, Bethany R.; Pickford, Helena D.; Rabe, Patrick; Sterling, Alistair J.; Zarganes-Tzitzikas, Tryfon; Grimes, Thomas; Thompson, Amber L.; Smith, Russell C.; Schofield, Christopher J.; Brennan, Paul E.; Duarte, Fernanda; Anderson, Edward A. (2022). "Synthesis of meta-substituted arene bioisosteres from [3.1.1]propellane". Nature. 611 (7937): 721–726. doi:10.1038/s41586-022-05290-z. PMID 36108675. S2CID 252310498.
  • Stepan, Antonia F.; et al. (2012). "Application of the Bicyclo[1.1.1]pentane Motif as a Nonclassical Phenyl Ring Bioisostere in the Design of a Potent and Orally Active γ-Secretase Inhibitor". J. Med. Chem. 55 (7): 3414–3424. doi:10.1021/jm300094u. PMID 22420884.
  • Jarosch, Oliver; Szeimies, Günter (2003). "Thermal Behavior of [2.1.1]Propellane: A DFT/Ab Initio Study". J. Org. Chem. 68 (10): 3797–3801. doi:10.1021/jo020741d. PMID 12737556.
  • Schmiedel, V. M.; Hong, Y. J.; Lentz, D; Tantillo, D. J.; Christmann, M (2018). "Synthesis and Structure Revision of Dichrocephones A and B". Angew. Chem. Int. Ed. 57 (9): 2419–2422. doi:10.1002/anie.201711766. PMID 29251825.
  • Schneider, L. M.; Schmiedel, V. M.; Pecchioli, T; Lentz, T; Merten, C; Christmann, M (2017). "Asymmetric Synthesis of Carbocyclic Propellanes". Org. Lett. 19 (9): 2310–2313. doi:10.1021/acs.orglett.7b00836. PMID 28445060.
  • Yang, Jian-Xiong; Wang, Yan Alexander (2021). "How Long Can a C–C σ-Single Bond Be?". The Journal of Physical Chemistry A. 125 (4): 933–942. doi:10.1021/acs.jpca.0c08924. PMID 33474940.

ncbi.nlm.nih.gov

semanticscholar.org (Global: 11th place; English: 8th place)

api.semanticscholar.org

  • Frank, Nils; Nugent, Jeremy; Shire, Bethany R.; Pickford, Helena D.; Rabe, Patrick; Sterling, Alistair J.; Zarganes-Tzitzikas, Tryfon; Grimes, Thomas; Thompson, Amber L.; Smith, Russell C.; Schofield, Christopher J.; Brennan, Paul E.; Duarte, Fernanda; Anderson, Edward A. (2022). "Synthesis of meta-substituted arene bioisosteres from [3.1.1]propellane". Nature. 611 (7937): 721–726. doi:10.1038/s41586-022-05290-z. PMID 36108675. S2CID 252310498.