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Synthesis and Solvolysis of 1-Bromobicyclo[1.1.1]pentane

EW Della and DK Taylor
43(5) pp.945 - 948


17 articles found in Crossref database.

Experimental and theoretical study of substituent effects on3J(13C1-1H) coupling constants in 1-X-bicyclo[1.1.1]pentanes
Della Ernest W., Lochert Ian J., Peruchena N�lida M., Aucar Gustavo A., Contreras Rub�n H.
Journal of Physical Organic Chemistry. 1996 9(3). p.168
Electrophilic Activation of [1.1.1]Propellane for the Synthesis of Nitrogen‐Substituted Bicyclo[1.1.1]pentanes
Livesley Sarah, Sterling Alistair J., Robertson Craig M., Goundry William R. F., Morris James A., Duarte Fernanda, Aïssa Christophe
Angewandte Chemie International Edition. 2022 61(2).
Inductive charge dispersal in the solvolysis of 3-substituted bicyclo[1.1.1] pentyl bromides
Grob Cyril A., Yang Cheng Xi, Della Ernest W., Taylor Dennis K.
Tetrahedron Letters. 1991 32(42). p.5945
Structure, stabilization energies and chemical shifts of the cyclobutenyl cation. Does it have ‘aromatic’ homocyclopropenium ion character? An ab initio study
Sieber Stefan, Schleyer Paul v. R., Otto André Henry, Gauss Jürgen, Reichel Felix, Cremer Dieter
Journal of Physical Organic Chemistry. 1993 6(8). p.445
Dearomative intermolecular [2 + 2] photocycloaddition for construction of C(sp3)-rich heterospirocycles on-DNA
Li Longbo, Matsuo Bianca, Levitre Guillaume, McClain Edward J., Voight Eric A., Crane Erika A., Molander Gary A.
Chemical Science. 2023 14(10). p.2713
Manifestations of Bridgehead−Bridgehead Interactions in the Bicyclo[1.1.1]pentane Ring System
Adcock William, Blokhin Andrei V., Elsey Gordon M., Head Nicholas H., Krstic Alexander R., Levin Michael D., Michl Josef, Munton Jamie, Pinkhassik Evgueni, Robert Marc, Savéant Jean-Michel, Shtarev Alexander, Stibor Ivan
The Journal of Organic Chemistry. 1999 64(8). p.2618
Re-Examination of Some Carbocations. Structures, Energies, and Charge Distributions
Wiberg Kenneth B., Rablen Paul R.
The Journal of Organic Chemistry. 2020 85(18). p.11741
Electrophilic Activation of [1.1.1]Propellane for the Synthesis of Nitrogen‐Substituted Bicyclo[1.1.1]pentanes
Livesley Sarah, Sterling Alistair J., Robertson Craig M., Goundry William R. F., Morris James A., Duarte Fernanda, Aïssa Christophe
Angewandte Chemie. 2022 134(2).
Patai's Chemistry of Functional Groups (2009)
Kaszynski Piotr, Michl Josef
Selected Topics in the Syntheses of Bicyclo[1.1.1]Pentane (BCP) Analogues
Ma Xiaoshen, Nhat Pham Luu
Asian Journal of Organic Chemistry. 2020 9(1). p.8
Strain and structural effects on rates of formation and stability of tertiary carbenium ions in the light of molecular mechanics calculations
Müller Paul, Mareda Jiri, Milin Didier
Journal of Physical Organic Chemistry. 1995 8(8). p.507
Comprehensive Study of the Methyl Effect on the Solvolysis Rates of Bridgehead Derivatives
Martínez Antonio García, Vilar Enrique Teso, Barcina José Osío, de la Moya Cerero Santiago
Journal of the American Chemical Society. 2002 124(23). p.6676
Bicyclo[1.1.1]pentanes, [n]Staffanes, [1.1.1]Propellanes, and Tricyclo[2.1.0.02,5]pentanes
Levin Michael D., Kaszynski Piotr, Michl Josef
Chemical Reviews. 2000 100(1). p.169
SYNTHESIS OF BIUDGEHEAD-SUBSTTTUTED BICYCLO[1.1.1]PENTANES. A REVIEW
Delia Ernest W., Lochert Ian J.
Organic Preparations and Procedures International. 1996 28(4). p.411
Synthesis of novel cage quaternary salts via nucleophilic substitution of 1,3-diiodobicyclo[1.1.1]pentane. Further evidence for a stable 3-iodo-1-bicyclo[1.1.1]pentyl cation.
Adcock James L., Gakh Andrei A.
Tetrahedron Letters. 1992 33(34). p.4875
Unusual bridgehead reactivity: Formation of [1.1.1]Propellane by 1,3-dehydrobromination of 1-bromobicyclo[1.1.1]Pentane.
Della Ernest W., Taylor Dennis K., Tsanaktsidis John
Tetrahedron Letters. 1990 31(36). p.5219
Ab initio and experimental study of NMR coupling constants in bicyclo[1.1.1]pentane
Lazzeretti Paolo, Malagoli Massimo, Zanasi Riccardo, Delia Ernest W., Lochert Ian J., Giribet Claudia G., de Azúa Martín C. Ruiz, Contreras Rubén H.
J. Chem. Soc., Faraday Trans.. 1995 91(22). p.4031

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