Robinson annulation (English Wikipedia)

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

refsWebsite

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14doi.org

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4nih.gov

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1nature.com

234^th place

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1harvard.edu

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1semanticscholar.org

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doi.org

Rapson, William Sage; Robinson, Robert (1935). "307. Experiments on the synthesis of substances related to the sterols. Part II. A new general method for the synthesis of substituted cyclohexenones". Journal of the Chemical Society (Resumed): 1285. doi:10.1039/JR9350001285.
Heathcock, Clayton H.; Ellis, John E.; McMurry, John E.; Coppolino, Anthony (1971). "Acid-catalyzed Robinson Annelations". Tetrahedron Letters. 12 (52): 4995–96. doi:10.1016/s0040-4039(01)97609-9.
Acheson, R. M.; Robinson, Robert (1952). "198. Experiments bearing on the synthesis of cortisone. Part I. Some cyclopentenone derivatives". Journal of the Chemical Society (Resumed): 1127. doi:10.1039/JR9520001127.
Gawley, Robert E. (1976). "The Robinson Annelation and Related Reactions". Synthesis. 1976 (12): 777–794. doi:10.1055/s-1976-24200.
Nussbaumer, Cornelius (1990). "Stereochemistry of the Robinson Anellation: Studies on the Mode of Formation of the Intermediate Hydroxy Ketones". Helvetica Chimica Acta. 73 (6): 1621–1636. doi:10.1002/hlca.19900730607.
Scanio, Charles J. V.; Starrett, Richmond M. (1971). "Remarkably stereoselective Robinson annulation reaction". Journal of the American Chemical Society. 93 (6): 1539–1540. doi:10.1021/ja00735a059.
Buchschacher, Paul; A. Fürst; J. Gutzwiller (1985). "(S)-8a-Methyl-3,4,8,8a-Tetrahydro-1,6(2H, 7H)-Napthalenedione". Organic Syntheses. 63: 37. doi:10.15227/orgsyn.063.0037.
Wang, Zerong (2009). "Wichterle Reaction". Comprehensive organic name reactions and reagents. Hoboken, N.J.: John Wiley. pp. 3003–3007. doi:10.1002/9780470638859.conrr669. ISBN 978-0-470-63885-9.
Hauser, Frank M.; Rhee, Richard P. (1978). "New synthetic methods for the regioselective annelation of aromatic rings: 1-hydroxy-2,3-disubstituted naphthalenes and 1,4-dihydroxy-2,3-disubstituted naphthalenes". The Journal of Organic Chemistry. 43 (1): 178–180. doi:10.1021/jo00395a048.
Eder, Ulrich; Sauer, Gerhard; Wiechert, Rudolf (1971). "New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures". Angewandte Chemie International Edition in English. 10 (7): 496–497. doi:10.1002/anie.197104961.
Bui, Tommy; Barbas, Carlos F (2000). "A proline-catalyzed asymmetric Robinson annulation reaction". Tetrahedron Letters. 41 (36): 6951–6954. doi:10.1016/s0040-4039(00)01180-1.
Linghu, X.; Kenedy-Smith, J. J.; Toste, F. D. (2007). "Total Synthesis of (+)-Fawcettimine". Angew. Chem. Int. Ed. 46 (40): 7671–3. doi:10.1002/anie.200702695. PMID 17729226.
Wang, Jun; Soisson, Stephen M.; Singh, Sheo; et al. (2006). "Platensimycin is a selective FabF inhibitor with potent antibiotic properties". Nature. 441 (7091): 358–61. Bibcode:2006Natur.441..358W. doi:10.1038/nature04784. PMID 16710421. S2CID 4329677. Retrieved 9 September 2021.
Li, Pingfan; Payette, Joshua N.; Yamamoto, Hisashi (2007). "Enantioselective Route to Platensimycin: An Intramolecular Robinson Annulation Approach". Journal of the American Chemical Society. 129 (31): 9534–9535. doi:10.1021/ja073547n. PMC 2553032. PMID 17630748.

harvard.edu

ui.adsabs.harvard.edu

Wang, Jun; Soisson, Stephen M.; Singh, Sheo; et al. (2006). "Platensimycin is a selective FabF inhibitor with potent antibiotic properties". Nature. 441 (7091): 358–61. Bibcode:2006Natur.441..358W. doi:10.1038/nature04784. PMID 16710421. S2CID 4329677. Retrieved 9 September 2021.

nature.com

Wang, Jun; Soisson, Stephen M.; Singh, Sheo; et al. (2006). "Platensimycin is a selective FabF inhibitor with potent antibiotic properties". Nature. 441 (7091): 358–61. Bibcode:2006Natur.441..358W. doi:10.1038/nature04784. PMID 16710421. S2CID 4329677. Retrieved 9 September 2021.

nih.gov

pubmed.ncbi.nlm.nih.gov

Linghu, X.; Kenedy-Smith, J. J.; Toste, F. D. (2007). "Total Synthesis of (+)-Fawcettimine". Angew. Chem. Int. Ed. 46 (40): 7671–3. doi:10.1002/anie.200702695. PMID 17729226.
Wang, Jun; Soisson, Stephen M.; Singh, Sheo; et al. (2006). "Platensimycin is a selective FabF inhibitor with potent antibiotic properties". Nature. 441 (7091): 358–61. Bibcode:2006Natur.441..358W. doi:10.1038/nature04784. PMID 16710421. S2CID 4329677. Retrieved 9 September 2021.
Li, Pingfan; Payette, Joshua N.; Yamamoto, Hisashi (2007). "Enantioselective Route to Platensimycin: An Intramolecular Robinson Annulation Approach". Journal of the American Chemical Society. 129 (31): 9534–9535. doi:10.1021/ja073547n. PMC 2553032. PMID 17630748.

ncbi.nlm.nih.gov

Li, Pingfan; Payette, Joshua N.; Yamamoto, Hisashi (2007). "Enantioselective Route to Platensimycin: An Intramolecular Robinson Annulation Approach". Journal of the American Chemical Society. 129 (31): 9534–9535. doi:10.1021/ja073547n. PMC 2553032. PMID 17630748.

semanticscholar.org

api.semanticscholar.org

Wang, Jun; Soisson, Stephen M.; Singh, Sheo; et al. (2006). "Platensimycin is a selective FabF inhibitor with potent antibiotic properties". Nature. 441 (7091): 358–61. Bibcode:2006Natur.441..358W. doi:10.1038/nature04784. PMID 16710421. S2CID 4329677. Retrieved 9 September 2021.