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Process chemistry (English Wikipedia)

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

refsWebsite
Global rank English rank
14doi.org
2nd place
2nd place
12nih.gov
4th place
4th place
2harvard.edu
18th place
17th place
2semanticscholar.org
11th place
8th place
1rug.nl
2,779th place
1,997th place
1handle.net
102nd place
76th place

doi.org

  • Roughley, S. D.; Jordan, A. M. (2011). "The medicinal chemist's toolbox: an analysis of reactions used in the pursuit of drug candidates". J. Med. Chem. 54 (10): 3451–79. doi:10.1021/jm200187y. PMID 21504168.
  • Dach, R.; Song, J. J.; Roschangar, F.; Samstag, W.; Senanayake, C. H. (2012). "The eight criteria defining a good chemical manufacturing process". Org. Process Res. Dev. 16 (11): 1697–1706. doi:10.1021/op300144g.
  • Trost, B. M. (1991). "The atom economy - a search for synthetic efficiency". Science. 254 (5037): 1471–7. Bibcode:1991Sci...254.1471T. doi:10.1126/science.1962206. PMID 1962206.
  • Van Aken, K.; Strekowski, L.; Patiny, L. (2006). "EcoScale, a semi-quantitative tool to select an organic preparation based on economical and ecological parameters". Beilstein J. Org. Chem. 2 (3): 3. doi:10.1186/1860-5397-2-3. PMC 1409775. PMID 16542013.
  • Faucher, A-M.; Bailey, M. D.; Beaulieu, P. L.; Brochu, C.; Duceppe, J-S.; Ferland, J-M.; Ghiro, E.; Gorys, V.; Halmos, T.; Kawai, S. H.; Poirier, M.; Simoneau, B.; Tsantrizos, Y. S.; Llinas-Brunet, M. (2004). "Synthesis of BILN 2061, an HCV NS3 protease inhibitor with proven antiviral effect in humans". Org. Lett. 6 (17): 2901–2904. doi:10.1021/ol0489907. PMID 15330643.
  • Yee, N. K.; Farina, V.; Houpis, I. N.; Haddad, N.; Frutos, R. P.; Gallou, F.; Wang, X-J.; Wei, X.; Simpson, R. D.; Feng, X.; Fuchs, V.; Xu, Y.; Tan, J.; Zhang, L.; Xu, J.; Smith-Keenan, L. L.; Vitous, J.; Ridges, M. D.; Spinelli, E. M.; Johnson, M. (2006). "Efficient large-scale synthesis of BILN 2061, a potent HCV protease inhibitor, by a convergent approach based on ring-closing metathesis". J. Org. Chem. 71 (19): 7133–7145. doi:10.1021/jo060285j. PMID 16958506.
  • Zeng, X.; Wei, X.; Farina, V.; Napolitano, E.; Xu, Y.; Zhang, L.; Haddad, N.; Yee, N. K.; Grinberg, N.; Shen, S.; Senanayake, C. H. (2006). "Epimerization reaction of a substituted vinylcyclopropane catalyzed by ruthenium carbenes: mechanistic analysis". J. Org. Chem. 71 (23): 8864–8875. doi:10.1021/jo061587o. PMID 17081017.
  • Grela, K.; Harutyunyan, S.; Michrowska, A. (2002). "A highly efficient ruthenium catalyst for metathesis reactions" (PDF). Angew. Chem. Int. Ed. 41 (21): 4038–4040. doi:10.1002/1521-3773(20021104)41:21<4038::aid-anie4038>3.0.co;2-0. hdl:11370/969f537e-6d3b-425c-abfa-1b41e7d0e330. PMID 12412074.
  • Wei, X.; Shu, C.; Haddad, N.; Zeng, X.; Patel, N. D.; Tan, Z.; Liu, J.; Lee, H.; Shen, S.; Campbell, S.; Varsolona, R. J.; Busacca, C. A.; Hossain, A.; Yee, N. K.; Senanayake, C. H. (2013). "A highly convergent and efficient synthesis of a macrocyclic hepatitis C virus protease inhibitor BI 201302". Org. Lett. 15 (5): 1016–1019. doi:10.1021/ol303498m. PMID 23406520.
  • Bornscheuer, U. T.; Huisman, G. W.; Kazlauskas, R. J.; Lutz, S.; Moore, J. C.; Robins, K. (2012). "Engineering the third wave of biocatalysis". Nature. 485 (7397): 185–94. Bibcode:2012Natur.485..185B. doi:10.1038/nature11117. PMID 22575958. S2CID 4379415.
  • Savile, C. K.; Janey, J. M.; Mundorff, E. C.; Moore, J. C.; Tam, S.; Jarvis, W. R.; Colback, J. C.; Krebber, A.; Fleitz, F. J.; Brands, J.; Devine, P. N.; Huisman, G. W.; Hughes, G. J. (2010). "Biocatalytic asymmetric synthesis of chiral amines applied to sitagliptin manufacture". Science. 329 (5989): 305–309. doi:10.1126/science.1188934. PMID 20558668. S2CID 21954817.
  • Desai, A. A. (2011). "Sitagliptin manufacture: a compelling tale of green chemistry, process intensification, and industrial asymmetric catalysis". Angew. Chem. Int. Ed. 50 (9): 1974–1976. doi:10.1002/anie.201007051. PMID 21284073.
  • Busacca, C. A.; Fandrick, D. R.; Song, J. J.; Sananayake, C. H. (2011). "The growing impact of catalysis in the pharmaceutical industry". Adv. Synth. Catal. 353 (11–12): 1825–1864. doi:10.1002/adsc.201100488.
  • Johnson, M. D.; May, S. A.; Calvin, J. R.; Remacle, J.; Stout, J. R.; Dieroad, W. D.; Zaborenko, N.; Haeberle, B. D.; Sun, W-M.; Miller, M. T.; Brannan, J. (2012). "Development and scale-up of a continuous, high-pressure, asymmetric hydrogenation reaction, workup, and isolation". Org. Process Res. Dev. 16 (5): 1017–1038. doi:10.1021/op200362h.

handle.net

hdl.handle.net

harvard.edu

ui.adsabs.harvard.edu

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Roughley, S. D.; Jordan, A. M. (2011). "The medicinal chemist's toolbox: an analysis of reactions used in the pursuit of drug candidates". J. Med. Chem. 54 (10): 3451–79. doi:10.1021/jm200187y. PMID 21504168.
  • Trost, B. M. (1991). "The atom economy - a search for synthetic efficiency". Science. 254 (5037): 1471–7. Bibcode:1991Sci...254.1471T. doi:10.1126/science.1962206. PMID 1962206.
  • Van Aken, K.; Strekowski, L.; Patiny, L. (2006). "EcoScale, a semi-quantitative tool to select an organic preparation based on economical and ecological parameters". Beilstein J. Org. Chem. 2 (3): 3. doi:10.1186/1860-5397-2-3. PMC 1409775. PMID 16542013.
  • Faucher, A-M.; Bailey, M. D.; Beaulieu, P. L.; Brochu, C.; Duceppe, J-S.; Ferland, J-M.; Ghiro, E.; Gorys, V.; Halmos, T.; Kawai, S. H.; Poirier, M.; Simoneau, B.; Tsantrizos, Y. S.; Llinas-Brunet, M. (2004). "Synthesis of BILN 2061, an HCV NS3 protease inhibitor with proven antiviral effect in humans". Org. Lett. 6 (17): 2901–2904. doi:10.1021/ol0489907. PMID 15330643.
  • Yee, N. K.; Farina, V.; Houpis, I. N.; Haddad, N.; Frutos, R. P.; Gallou, F.; Wang, X-J.; Wei, X.; Simpson, R. D.; Feng, X.; Fuchs, V.; Xu, Y.; Tan, J.; Zhang, L.; Xu, J.; Smith-Keenan, L. L.; Vitous, J.; Ridges, M. D.; Spinelli, E. M.; Johnson, M. (2006). "Efficient large-scale synthesis of BILN 2061, a potent HCV protease inhibitor, by a convergent approach based on ring-closing metathesis". J. Org. Chem. 71 (19): 7133–7145. doi:10.1021/jo060285j. PMID 16958506.
  • Zeng, X.; Wei, X.; Farina, V.; Napolitano, E.; Xu, Y.; Zhang, L.; Haddad, N.; Yee, N. K.; Grinberg, N.; Shen, S.; Senanayake, C. H. (2006). "Epimerization reaction of a substituted vinylcyclopropane catalyzed by ruthenium carbenes: mechanistic analysis". J. Org. Chem. 71 (23): 8864–8875. doi:10.1021/jo061587o. PMID 17081017.
  • Grela, K.; Harutyunyan, S.; Michrowska, A. (2002). "A highly efficient ruthenium catalyst for metathesis reactions" (PDF). Angew. Chem. Int. Ed. 41 (21): 4038–4040. doi:10.1002/1521-3773(20021104)41:21<4038::aid-anie4038>3.0.co;2-0. hdl:11370/969f537e-6d3b-425c-abfa-1b41e7d0e330. PMID 12412074.
  • Wei, X.; Shu, C.; Haddad, N.; Zeng, X.; Patel, N. D.; Tan, Z.; Liu, J.; Lee, H.; Shen, S.; Campbell, S.; Varsolona, R. J.; Busacca, C. A.; Hossain, A.; Yee, N. K.; Senanayake, C. H. (2013). "A highly convergent and efficient synthesis of a macrocyclic hepatitis C virus protease inhibitor BI 201302". Org. Lett. 15 (5): 1016–1019. doi:10.1021/ol303498m. PMID 23406520.
  • Bornscheuer, U. T.; Huisman, G. W.; Kazlauskas, R. J.; Lutz, S.; Moore, J. C.; Robins, K. (2012). "Engineering the third wave of biocatalysis". Nature. 485 (7397): 185–94. Bibcode:2012Natur.485..185B. doi:10.1038/nature11117. PMID 22575958. S2CID 4379415.
  • Savile, C. K.; Janey, J. M.; Mundorff, E. C.; Moore, J. C.; Tam, S.; Jarvis, W. R.; Colback, J. C.; Krebber, A.; Fleitz, F. J.; Brands, J.; Devine, P. N.; Huisman, G. W.; Hughes, G. J. (2010). "Biocatalytic asymmetric synthesis of chiral amines applied to sitagliptin manufacture". Science. 329 (5989): 305–309. doi:10.1126/science.1188934. PMID 20558668. S2CID 21954817.
  • Desai, A. A. (2011). "Sitagliptin manufacture: a compelling tale of green chemistry, process intensification, and industrial asymmetric catalysis". Angew. Chem. Int. Ed. 50 (9): 1974–1976. doi:10.1002/anie.201007051. PMID 21284073.

ncbi.nlm.nih.gov

rug.nl

pure.rug.nl

semanticscholar.org

api.semanticscholar.org