Tropinone (English Wikipedia)

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

refsWebsite

Global rank English rank

12doi.org

2^nd place

8nih.gov

4^th place

3harvard.edu

18^th place

17^th place

1europa.eu

68^th place

117^th place

1zenodo.org

621^st place

380^th place

1ebi.ac.uk

5,849^th place

7,886^th place

1jstor.org

26^th place

20^th place

1semanticscholar.org

11^th place

8^th place

1patents.google.com

1,182^nd place

725^th place

1worldcat.org

5^th place

doi.org

Robinson R (1917). "LXIII. A Synthesis of Tropinone". Journal of the Chemical Society, Transactions. 111: 762–768. doi:10.1039/CT9171100762.
Nicolaou KC, Vourloumis D, Winssinger N, Baran PS (2000). "The Art and Science of Total Synthesis at the Dawn of the Twenty-First Century". Angewandte Chemie International Edition. 39 (1): 44–122. doi:10.1002/(SICI)1521-3773(20000103)39:1<44::AID-ANIE44>3.0.CO;2-L. PMID 10649349.
Smit WA, Smit WA, Bochkov AF, Caple R (1998). Organic Synthesis. doi:10.1039/9781847551573. ISBN 978-0-85404-544-0.
Humphrey AJ, O'Hagan D (2001). "Tropane alkaloid biosynthesis. A century old problem unresolved". Natural Product Reports. 18 (5). Royal Society of Chemistry: 494–502. doi:10.1039/b001713m. PMID 11699882.
Birch AJ (1993). "Investigating a Scientific Legend: The Tropinone Synthesis of Sir Robert Robinson, F.R.S". Notes and Records of the Royal Society of London. 47 (2): 277–296. doi:10.1098/rsnr.1993.0034. JSTOR 531792. S2CID 143267467.
Wang S, Sakamuri S, Enyedy IJ, Kozikowski AP, Deschaux O, Bandyopadhyay BC, Tella SR, Zaman WA, Johnson KM (2000). "Discovery of a novel dopamine transporter inhibitor, 4-hydroxy-1-methyl-4-(4-methylphenyl)-3-piperidyl 4-methylphenyl ketone, as a potential cocaine antagonist through 3D-database pharmacophore searching. Molecular modeling, structure-activity relationships, and behavioral pharmacological studies". Journal of Medicinal Chemistry. 43 (3): 351–360. doi:10.1021/jm990516x. PMID 10669562.
Wang S, Sakamuri, Enyedy, Kozikowski, Zaman, Johnson (2001). "Molecular modeling, structure--activity relationships and functional antagonism studies of 4-hydroxy-1-methyl-4-(4-methylphenyl)-3-piperidyl 4-methylphenyl ketones as a novel class of dopamine transporter inhibitors". Bioorganic & Medicinal Chemistry. 9 (7): 1753–1764. doi:10.1016/S0968-0896(01)00090-6. PMID 11425577.
Findlay SP (1957). "Concerning 2-Carbomethoxytropinone". Journal of Organic Chemistry. 22 (11): 1385–1394. doi:10.1021/jo01362a022.
Nicolaou KC, Montagnon T, Baran PS, Zhong YL (2002). "Iodine(V) reagents in organic synthesis. Part 4. O-Iodoxybenzoic acid as a chemospecific tool for single electron transfer-based oxidation processes". Journal of the American Chemical Society. 124 (10): 2245–58. doi:10.1021/ja012127+. PMID 11878978.
Bedewitz MA, Jones AD, D'Auria JC, Barry CS (2018). "Tropinone synthesis via an atypical polyketide synthase and P450-mediated cyclization". Nature Communications. 9 (1): 5281. Bibcode:2018NatCo...9.5281B. doi:10.1038/s41467-018-07671-3. ISSN 2041-1723. PMC 6290073. PMID 30538251.
A. Portsteffen, B. Draeger, A. Nahrstedt (1992). "Two tropinone reducing enzymes from Datura stramonium transformed root cultures". Phytochemistry. 31 (4): 1135. Bibcode:1992PChem..31.1135P. doi:10.1016/0031-9422(92)80247-C.
Boswell HD, Dräger B, McLauchlan WR, et al. (November 1999). "Specificities of the enzymes of N-alkyltropane biosynthesis in Brugmansia and Datura". Phytochemistry. 52 (5): 871–8. Bibcode:1999PChem..52..871B. doi:10.1016/S0031-9422(99)00293-9. PMID 10626376.

ebi.ac.uk

Chemical Entities of Biological Interest Identification code: ChEBI:57851 "tropiniumone"

europa.eu

echa.europa.eu

"Tropinone". Substance Information. ECHA.

harvard.edu

ui.adsabs.harvard.edu

Bedewitz MA, Jones AD, D'Auria JC, Barry CS (2018). "Tropinone synthesis via an atypical polyketide synthase and P450-mediated cyclization". Nature Communications. 9 (1): 5281. Bibcode:2018NatCo...9.5281B. doi:10.1038/s41467-018-07671-3. ISSN 2041-1723. PMC 6290073. PMID 30538251.
A. Portsteffen, B. Draeger, A. Nahrstedt (1992). "Two tropinone reducing enzymes from Datura stramonium transformed root cultures". Phytochemistry. 31 (4): 1135. Bibcode:1992PChem..31.1135P. doi:10.1016/0031-9422(92)80247-C.
Boswell HD, Dräger B, McLauchlan WR, et al. (November 1999). "Specificities of the enzymes of N-alkyltropane biosynthesis in Brugmansia and Datura". Phytochemistry. 52 (5): 871–8. Bibcode:1999PChem..52..871B. doi:10.1016/S0031-9422(99)00293-9. PMID 10626376.

jstor.org

Birch AJ (1993). "Investigating a Scientific Legend: The Tropinone Synthesis of Sir Robert Robinson, F.R.S". Notes and Records of the Royal Society of London. 47 (2): 277–296. doi:10.1098/rsnr.1993.0034. JSTOR 531792. S2CID 143267467.

nih.gov

pubmed.ncbi.nlm.nih.gov

Nicolaou KC, Vourloumis D, Winssinger N, Baran PS (2000). "The Art and Science of Total Synthesis at the Dawn of the Twenty-First Century". Angewandte Chemie International Edition. 39 (1): 44–122. doi:10.1002/(SICI)1521-3773(20000103)39:1<44::AID-ANIE44>3.0.CO;2-L. PMID 10649349.
Humphrey AJ, O'Hagan D (2001). "Tropane alkaloid biosynthesis. A century old problem unresolved". Natural Product Reports. 18 (5). Royal Society of Chemistry: 494–502. doi:10.1039/b001713m. PMID 11699882.
Wang S, Sakamuri S, Enyedy IJ, Kozikowski AP, Deschaux O, Bandyopadhyay BC, Tella SR, Zaman WA, Johnson KM (2000). "Discovery of a novel dopamine transporter inhibitor, 4-hydroxy-1-methyl-4-(4-methylphenyl)-3-piperidyl 4-methylphenyl ketone, as a potential cocaine antagonist through 3D-database pharmacophore searching. Molecular modeling, structure-activity relationships, and behavioral pharmacological studies". Journal of Medicinal Chemistry. 43 (3): 351–360. doi:10.1021/jm990516x. PMID 10669562.
Wang S, Sakamuri, Enyedy, Kozikowski, Zaman, Johnson (2001). "Molecular modeling, structure--activity relationships and functional antagonism studies of 4-hydroxy-1-methyl-4-(4-methylphenyl)-3-piperidyl 4-methylphenyl ketones as a novel class of dopamine transporter inhibitors". Bioorganic & Medicinal Chemistry. 9 (7): 1753–1764. doi:10.1016/S0968-0896(01)00090-6. PMID 11425577.
Nicolaou KC, Montagnon T, Baran PS, Zhong YL (2002). "Iodine(V) reagents in organic synthesis. Part 4. O-Iodoxybenzoic acid as a chemospecific tool for single electron transfer-based oxidation processes". Journal of the American Chemical Society. 124 (10): 2245–58. doi:10.1021/ja012127+. PMID 11878978.
Bedewitz MA, Jones AD, D'Auria JC, Barry CS (2018). "Tropinone synthesis via an atypical polyketide synthase and P450-mediated cyclization". Nature Communications. 9 (1): 5281. Bibcode:2018NatCo...9.5281B. doi:10.1038/s41467-018-07671-3. ISSN 2041-1723. PMC 6290073. PMID 30538251.
Boswell HD, Dräger B, McLauchlan WR, et al. (November 1999). "Specificities of the enzymes of N-alkyltropane biosynthesis in Brugmansia and Datura". Phytochemistry. 52 (5): 871–8. Bibcode:1999PChem..52..871B. doi:10.1016/S0031-9422(99)00293-9. PMID 10626376.

ncbi.nlm.nih.gov

Bedewitz MA, Jones AD, D'Auria JC, Barry CS (2018). "Tropinone synthesis via an atypical polyketide synthase and P450-mediated cyclization". Nature Communications. 9 (1): 5281. Bibcode:2018NatCo...9.5281B. doi:10.1038/s41467-018-07671-3. ISSN 2041-1723. PMC 6290073. PMID 30538251.

patents.google.com

U.S. patent 8,609,690

semanticscholar.org

api.semanticscholar.org

Birch AJ (1993). "Investigating a Scientific Legend: The Tropinone Synthesis of Sir Robert Robinson, F.R.S". Notes and Records of the Royal Society of London. 47 (2): 277–296. doi:10.1098/rsnr.1993.0034. JSTOR 531792. S2CID 143267467.

worldcat.org

search.worldcat.org

Bedewitz MA, Jones AD, D'Auria JC, Barry CS (2018). "Tropinone synthesis via an atypical polyketide synthase and P450-mediated cyclization". Nature Communications. 9 (1): 5281. Bibcode:2018NatCo...9.5281B. doi:10.1038/s41467-018-07671-3. ISSN 2041-1723. PMC 6290073. PMID 30538251.

zenodo.org

Robinson R (1917). "LXIII. A Synthesis of Tropinone". Journal of the Chemical Society, Transactions. 111: 762–768. doi:10.1039/CT9171100762.