Bullvalene (English Wikipedia)

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

refsWebsite

Global rank English rank

12doi.org

2^nd place

7harvard.edu

18^th place

17^th place

4nih.gov

4^th place

2worldcat.org

5^th place

1wiley.com

222^nd place

297^th place

1books.google.com

3^rd place

1mcmaster.ca

6,572^nd place

4,351^st place

1web.archive.org

1^st place

books.google.com (Global: 3^rd place; English: 3^rd place)

Alex Nickon, Ernest F. Silversmith, Organic Chemistry: The Name Game: Modern Coined Terms and Their Origins, p. 133, Pergamon Press, 1987.

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

Addison Ault (2001). "The Bullvalene Story. The Conception of Bullvalene, a Molecule That Has No Permanent Structure". Journal of Chemical Education. 78 (7): 924. Bibcode:2001JChEd..78..924A. doi:10.1021/ed078p924.
Oth, J.; Mullen, K.; Gilles, J.; Schröder, G. (1974). "Comparison of 13C- and 1H- magnetic resonance spectroscopy as techniques for the quantitative investigation of dynamic processes. The Cope rearrangement in bullvalene". Helv Chim Acta. 57 (5): 1415–1433. doi:10.1002/hlca.19740570518.
Ives, Robert A.; Maturi, William; Gill, Matthew T.; Rankine, Conor; McGonigal, Paul R. (2024-09-18). "A guide to bullvalene stereodynamics". Chemical Science. 15 (36): 14608–14617. doi:10.1039/D4SC03700F. ISSN 2041-6539. PMC 11358867. PMID 39220163.
Schröder, Gerhard (1963). "Preparation and Properties of Tricyclo[3,3,2,04,6]deca-2,7,9-triene (Bullvalene)". Angewandte Chemie International Edition in English. 2 (8): 481–482. doi:10.1002/anie.196304814. ISSN 0570-0833.
Von Eggers Doering, W.; Rosenthal, Joel W. (1966). "9,10-Dihydronaphthalene. Formation from Bullvalene and Nenitzescu's Hydrocarbon, Thermal Reorganization, and Photorearrangement to Bullvalene". J. Am. Chem. Soc. 88 (9): 2078–2079. Bibcode:1966JAChS..88.2078V. doi:10.1021/ja00961a061.
Lippert, A. R.; Kaeobamrung, J.; Bode, J. W. (2006). "Synthesis of Oligosubstituted Bullvalones: Shapeshifting Molecules Under Basic Conditions". J. Am. Chem. Soc. 128 (46): 14738–14739. Bibcode:2006JAChS.12814738L. doi:10.1021/ja063900+. PMID 17105247.
Zimmerman, H. E.; Grunewald, G. L. (1966). "The Chemistry of Barrelene. III. A Unique Photoisomerization to Semibullvalene". J. Am. Chem. Soc. 88 (1): 183–184. Bibcode:1966JAChS..88..183Z. doi:10.1021/ja00953a045.
Zimmerman, H. E.; Binkley, R. W.; Givens, R. S.; Sherwin, M. A. (1967). "Mechanistic Organic Photochemistry. XXIV. The Mechanism of the Conversion of Barrelene to Semibullvalene. A General Photochemical Process". J. Am. Chem. Soc. 89 (15): 3932–3933. Bibcode:1967JAChS..89.3932Z. doi:10.1021/ja00991a064.
Wang, C.; Yuan, J.; Li, G.; Wang, Z.; Zhang, S.; Xi, Z. (2006). "Metal-Mediated Efficient Synthesis, Structural Characterization, and Skeletal Rearrangement of Octasubstituted Semibullvalenes". J. Am. Chem. Soc. 128 (14): 4564–4565. Bibcode:2006JAChS.128.4564W. doi:10.1021/ja0579208. PMID 16594680.
Doering, W. von E.; Roth, W. R. (1963). "A Rapidly Reversible Degenerate Cope Rearrangement : Bicyclo[5.1.0]octa-2,5-diene". Tetrahedron. 19 (5): 715–737. doi:10.1016/S0040-4020(01)99207-5.^{[dead link]}
Ault, Addison (2001). "The Bullvalene Story. The Conception of Bullvalene, a Molecule That Has No Permanent Structure". J. Chem. Educ. 78 (7): 924. Bibcode:2001JChEd..78..924A. doi:10.1021/ed078p924.
Klärner, F.-G. (2011), William von Eggers Doering (1917–2011). Angewandte Chemie International Edition, 50: 2885–2886. doi:10.1002/anie.201100453

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

ui.adsabs.harvard.edu

Addison Ault (2001). "The Bullvalene Story. The Conception of Bullvalene, a Molecule That Has No Permanent Structure". Journal of Chemical Education. 78 (7): 924. Bibcode:2001JChEd..78..924A. doi:10.1021/ed078p924.
Von Eggers Doering, W.; Rosenthal, Joel W. (1966). "9,10-Dihydronaphthalene. Formation from Bullvalene and Nenitzescu's Hydrocarbon, Thermal Reorganization, and Photorearrangement to Bullvalene". J. Am. Chem. Soc. 88 (9): 2078–2079. Bibcode:1966JAChS..88.2078V. doi:10.1021/ja00961a061.
Lippert, A. R.; Kaeobamrung, J.; Bode, J. W. (2006). "Synthesis of Oligosubstituted Bullvalones: Shapeshifting Molecules Under Basic Conditions". J. Am. Chem. Soc. 128 (46): 14738–14739. Bibcode:2006JAChS.12814738L. doi:10.1021/ja063900+. PMID 17105247.
Zimmerman, H. E.; Grunewald, G. L. (1966). "The Chemistry of Barrelene. III. A Unique Photoisomerization to Semibullvalene". J. Am. Chem. Soc. 88 (1): 183–184. Bibcode:1966JAChS..88..183Z. doi:10.1021/ja00953a045.
Zimmerman, H. E.; Binkley, R. W.; Givens, R. S.; Sherwin, M. A. (1967). "Mechanistic Organic Photochemistry. XXIV. The Mechanism of the Conversion of Barrelene to Semibullvalene. A General Photochemical Process". J. Am. Chem. Soc. 89 (15): 3932–3933. Bibcode:1967JAChS..89.3932Z. doi:10.1021/ja00991a064.
Wang, C.; Yuan, J.; Li, G.; Wang, Z.; Zhang, S.; Xi, Z. (2006). "Metal-Mediated Efficient Synthesis, Structural Characterization, and Skeletal Rearrangement of Octasubstituted Semibullvalenes". J. Am. Chem. Soc. 128 (14): 4564–4565. Bibcode:2006JAChS.128.4564W. doi:10.1021/ja0579208. PMID 16594680.
Ault, Addison (2001). "The Bullvalene Story. The Conception of Bullvalene, a Molecule That Has No Permanent Structure". J. Chem. Educ. 78 (7): 924. Bibcode:2001JChEd..78..924A. doi:10.1021/ed078p924.

mcmaster.ca (Global: 6,572^nd place; English: 4,351^st place)

fhs.mcmaster.ca

A tribute to professor emeritus Barbara Ferrier Archived 2017-01-02 at the Wayback Machine, McMaster University, 6 January 2006

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

pubmed.ncbi.nlm.nih.gov

Ives, Robert A.; Maturi, William; Gill, Matthew T.; Rankine, Conor; McGonigal, Paul R. (2024-09-18). "A guide to bullvalene stereodynamics". Chemical Science. 15 (36): 14608–14617. doi:10.1039/D4SC03700F. ISSN 2041-6539. PMC 11358867. PMID 39220163.
Lippert, A. R.; Kaeobamrung, J.; Bode, J. W. (2006). "Synthesis of Oligosubstituted Bullvalones: Shapeshifting Molecules Under Basic Conditions". J. Am. Chem. Soc. 128 (46): 14738–14739. Bibcode:2006JAChS.12814738L. doi:10.1021/ja063900+. PMID 17105247.
Wang, C.; Yuan, J.; Li, G.; Wang, Z.; Zhang, S.; Xi, Z. (2006). "Metal-Mediated Efficient Synthesis, Structural Characterization, and Skeletal Rearrangement of Octasubstituted Semibullvalenes". J. Am. Chem. Soc. 128 (14): 4564–4565. Bibcode:2006JAChS.128.4564W. doi:10.1021/ja0579208. PMID 16594680.

ncbi.nlm.nih.gov

Ives, Robert A.; Maturi, William; Gill, Matthew T.; Rankine, Conor; McGonigal, Paul R. (2024-09-18). "A guide to bullvalene stereodynamics". Chemical Science. 15 (36): 14608–14617. doi:10.1039/D4SC03700F. ISSN 2041-6539. PMC 11358867. PMID 39220163.

web.archive.org (Global: 1^st place; English: 1^st place)

A tribute to professor emeritus Barbara Ferrier Archived 2017-01-02 at the Wayback Machine, McMaster University, 6 January 2006

wiley.com (Global: 222^nd place; English: 297^th place)

onlinelibrary.wiley.com

Schröder, Gerhard (1963). "Preparation and Properties of Tricyclo[3,3,2,04,6]deca-2,7,9-triene (Bullvalene)". Angewandte Chemie International Edition in English. 2 (8): 481–482. doi:10.1002/anie.196304814. ISSN 0570-0833.

worldcat.org (Global: 5^th place; English: 5^th place)

search.worldcat.org

Ives, Robert A.; Maturi, William; Gill, Matthew T.; Rankine, Conor; McGonigal, Paul R. (2024-09-18). "A guide to bullvalene stereodynamics". Chemical Science. 15 (36): 14608–14617. doi:10.1039/D4SC03700F. ISSN 2041-6539. PMC 11358867. PMID 39220163.
Schröder, Gerhard (1963). "Preparation and Properties of Tricyclo[3,3,2,04,6]deca-2,7,9-triene (Bullvalene)". Angewandte Chemie International Edition in English. 2 (8): 481–482. doi:10.1002/anie.196304814. ISSN 0570-0833.

Bullvalene (English Wikipedia)

books.google.com (Global: 3rd place; English: 3rd place)

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

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