Fluorenylmethyloxycarbonyl protecting group (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Fluorenylmethyloxycarbonyl protecting group" in English language version.

refsWebsite

Global rank English rank

9doi.org

2^nd place

4worldcat.org

5^th place

4nih.gov

4^th place

1acs.org

1,248^th place

1,104^th place

1sciencedirect.com

149^th place

178^th place

1harvard.edu

18^th place

17^th place

1semanticscholar.org

11^th place

8^th place

acs.org (Global: 1,248^th place; English: 1,104^th place)

pubs.acs.org

Carpino, Louis A.; Han, Grace Y. (November 1972). "9-Fluorenylmethoxycarbonyl amino-protecting group". The Journal of Organic Chemistry. 37 (22): 3404–3409. doi:10.1021/jo00795a005. ISSN 0022-3263.

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

Carpino, Louis A.; Han, Grace Y. (November 1972). "9-Fluorenylmethoxycarbonyl amino-protecting group". The Journal of Organic Chemistry. 37 (22): 3404–3409. doi:10.1021/jo00795a005. ISSN 0022-3263.
Várady, László; Rajur, Shranabasava B; Nicewonger, Robert B; Guo, MaoJun; Ditto, Lori (2000-02-11). "Fast and quantitative high-performance liquid chromatography method for the determination of 9-fluorenylmethoxycarbonyl release from solid-phase synthesis resins". Journal of Chromatography A. 869 (1): 171–179. doi:10.1016/S0021-9673(99)00844-4. ISSN 0021-9673. PMID 10720236.
Yamada, Kazuhiko; Hashizume, Daisuke; Shimizu, Tadashi; Ohki, Shinobu; Yokoyama, Shigeyuki (2008). "A solid-state 17O NMR, X-ray, and quantum chemical study of N-α-Fmoc-protected amino acids". Journal of Molecular Structure. 888 (1–3): 187–196. doi:10.1016/j.molstruc.2007.11.059.
Paquet, A. (1982). "Introduction of 9-fluorenylmethyloxycarbonyl, trichloroethoxycarbonyl, and benzyloxycarbonyl amine protecting groups into O-unprotected hydroxyamino acids using succinimidyl carbonates". Canadian Journal of Chemistry. 60 (8): 976–980. doi:10.1139/v82-146.
Fields, Gregg B. (1995), Pennington, Michael W.; Dunn, Ben M. (eds.), "Methods for Removing the Finoc Group", Peptide Synthesis Protocols, Methods in Molecular Biology, vol. 35, Totowa, NJ: Humana Press, pp. 17–27, doi:10.1385/0-89603-273-6:17, ISBN 978-1-59259-522-8, PMID 7894598, retrieved 2021-10-15{{citation}}: CS1 maint: work parameter with ISBN (link)
Wellings, Donald A.; Atherton, Eric (1997). "[4] Standard Fmoc protocols". Solid-Phase Peptide Synthesis. Methods in Enzymology. Vol. 289. pp. 44–67. doi:10.1016/s0076-6879(97)89043-x. ISBN 9780121821906. PMID 9353717.
Wuts, P. G. M.; Greene, T.W. (2006). Greene's Protective Groups in Organic Synthesis. NY: J. Wiley. doi:10.1002/0470053488. ISBN 9780470053485.
Ralhan, Krittika; KrishnaKumar, V. Guru; Gupta, Sharad (8 December 2015). "Piperazine and DBU: a safer alternative for rapid and efficient Fmoc deprotection in solid phase peptide synthesis". RSC Advances. 5 (126): 104417–104425. Bibcode:2015RSCAd...5j4417R. doi:10.1039/C5RA23441G. ISSN 2046-2069.
Lam, Pak-Lun; Wu, Yue; Wong, Ka-Leung (30 March 2022). "Incorporation of Fmoc-Dab(Mtt)-OH during solid-phase peptide synthesis: a word of caution". Organic & Biomolecular Chemistry. 20 (13): 2601–2604. doi:10.1039/D2OB00070A. ISSN 1477-0539. PMID 35258068. S2CID 247175352.

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

ui.adsabs.harvard.edu

Ralhan, Krittika; KrishnaKumar, V. Guru; Gupta, Sharad (8 December 2015). "Piperazine and DBU: a safer alternative for rapid and efficient Fmoc deprotection in solid phase peptide synthesis". RSC Advances. 5 (126): 104417–104425. Bibcode:2015RSCAd...5j4417R. doi:10.1039/C5RA23441G. ISSN 2046-2069.

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

pubmed.ncbi.nlm.nih.gov

Várady, László; Rajur, Shranabasava B; Nicewonger, Robert B; Guo, MaoJun; Ditto, Lori (2000-02-11). "Fast and quantitative high-performance liquid chromatography method for the determination of 9-fluorenylmethoxycarbonyl release from solid-phase synthesis resins". Journal of Chromatography A. 869 (1): 171–179. doi:10.1016/S0021-9673(99)00844-4. ISSN 0021-9673. PMID 10720236.
Fields, Gregg B. (1995), Pennington, Michael W.; Dunn, Ben M. (eds.), "Methods for Removing the Finoc Group", Peptide Synthesis Protocols, Methods in Molecular Biology, vol. 35, Totowa, NJ: Humana Press, pp. 17–27, doi:10.1385/0-89603-273-6:17, ISBN 978-1-59259-522-8, PMID 7894598, retrieved 2021-10-15{{citation}}: CS1 maint: work parameter with ISBN (link)
Wellings, Donald A.; Atherton, Eric (1997). "[4] Standard Fmoc protocols". Solid-Phase Peptide Synthesis. Methods in Enzymology. Vol. 289. pp. 44–67. doi:10.1016/s0076-6879(97)89043-x. ISBN 9780121821906. PMID 9353717.
Lam, Pak-Lun; Wu, Yue; Wong, Ka-Leung (30 March 2022). "Incorporation of Fmoc-Dab(Mtt)-OH during solid-phase peptide synthesis: a word of caution". Organic & Biomolecular Chemistry. 20 (13): 2601–2604. doi:10.1039/D2OB00070A. ISSN 1477-0539. PMID 35258068. S2CID 247175352.

sciencedirect.com (Global: 149^th place; English: 178^th place)

Várady, László; Rajur, Shranabasava B; Nicewonger, Robert B; Guo, MaoJun; Ditto, Lori (2000-02-11). "Fast and quantitative high-performance liquid chromatography method for the determination of 9-fluorenylmethoxycarbonyl release from solid-phase synthesis resins". Journal of Chromatography A. 869 (1): 171–179. doi:10.1016/S0021-9673(99)00844-4. ISSN 0021-9673. PMID 10720236.

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

api.semanticscholar.org

Lam, Pak-Lun; Wu, Yue; Wong, Ka-Leung (30 March 2022). "Incorporation of Fmoc-Dab(Mtt)-OH during solid-phase peptide synthesis: a word of caution". Organic & Biomolecular Chemistry. 20 (13): 2601–2604. doi:10.1039/D2OB00070A. ISSN 1477-0539. PMID 35258068. S2CID 247175352.

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

search.worldcat.org

Carpino, Louis A.; Han, Grace Y. (November 1972). "9-Fluorenylmethoxycarbonyl amino-protecting group". The Journal of Organic Chemistry. 37 (22): 3404–3409. doi:10.1021/jo00795a005. ISSN 0022-3263.
Várady, László; Rajur, Shranabasava B; Nicewonger, Robert B; Guo, MaoJun; Ditto, Lori (2000-02-11). "Fast and quantitative high-performance liquid chromatography method for the determination of 9-fluorenylmethoxycarbonyl release from solid-phase synthesis resins". Journal of Chromatography A. 869 (1): 171–179. doi:10.1016/S0021-9673(99)00844-4. ISSN 0021-9673. PMID 10720236.
Ralhan, Krittika; KrishnaKumar, V. Guru; Gupta, Sharad (8 December 2015). "Piperazine and DBU: a safer alternative for rapid and efficient Fmoc deprotection in solid phase peptide synthesis". RSC Advances. 5 (126): 104417–104425. Bibcode:2015RSCAd...5j4417R. doi:10.1039/C5RA23441G. ISSN 2046-2069.
Lam, Pak-Lun; Wu, Yue; Wong, Ka-Leung (30 March 2022). "Incorporation of Fmoc-Dab(Mtt)-OH during solid-phase peptide synthesis: a word of caution". Organic & Biomolecular Chemistry. 20 (13): 2601–2604. doi:10.1039/D2OB00070A. ISSN 1477-0539. PMID 35258068. S2CID 247175352.

Fluorenylmethyloxycarbonyl protecting group (English Wikipedia)

acs.org (Global: 1,248th place; English: 1,104th place)

pubs.acs.org

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

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