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Reaksi Diels–Alder (Indonesian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Reaksi Diels–Alder" in Indonesian language version.

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23doi.org
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2nih.gov
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1nobelprize.org
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1acs.org
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acs.org

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doi.org

  • Diels, O.; Alder, K. (1928). "Synthesen in der hydroaromatischen Reihe". Liebigs Annalen der Chemie. 460 (1): 98 – 122. doi:10.1002/jlac.19284600106. 
  • Karya Diels dan Alder terdiri dari seri 28 artikel yang ditulis dalam Bahasa Jerman yang dipublikasikan dalam Justus Liebigs Annalen der Chemie dan Berichte der deutschen chemischen Gesellschaft selama 10 tahun, sejak 1928 hingga 1937. Sembilan belas artikel pertama ditulis oleh Diels dan Alder, sedangkan artikel selanjutnya ditulis oleh Diels dan berbagai kontributor.
    • Diels, O.; Alder, K. (1928). "Synthesen in der hydroaromatischen Reihe, I". Justus Liebigs Annalen der Chemie. 460: 98–122. doi:10.1002/jlac.19284600106. 
    • Kloetzel, M. C. (1948). "The Diels-Alder Reaction with Maleic Anhydride". Organic Reactions. 4: 1–59. doi:10.1002/0471264180.or004.01. ISBN 0471264180. 
    • Holmes, H. L. (1948). "The Diels-Alder Reaction Ethylenic and Acetylenic Dienophiles". Organic Reactions. 4: 60–173. doi:10.1002/0471264180.or004.02. ISBN 0471264180. 
    • Nicolaou, K. C.; Snyder, S. A.; Montagnon, T.; Vassilikogiannakis, G. (2002). "The Diels-Alder Reaction in Total Synthesis". Angewandte Chemie International Edition. 41 (10): 1668–1698. doi:10.1002/1521-3773(20020517)41:10<1668::AID-ANIE1668>3.0.CO;2-Z. 
    • Dewar, M. J.; Olivella, S.; Stewart, J. J. (1986). "Mechanism of the Diels-Alder reaction: Reactions of butadiene with ethylene and cyanoethylenes". Journal of the American Chemical Society. 108 (19): 5771–5779. doi:10.1021/ja00279a018. PMID 22175326. 
    • Gajewski, J. J.; Peterson, K. B.; Kagel, J. R. (1987). "Transition-state structure variation in the Diels-Alder reaction from secondary deuterium kinetic isotope effects: The reaction of a nearly symmetrical diene and dienophile is nearly synchronous". Journal of the American Chemical Society. 109 (18): 5545–5546. doi:10.1021/ja00252a052. 
    • Houk, K. N.; Lin, Y. T.; Brown, F. K. (1986). "Evidence for the concerted mechanism of the Diels-Alder reaction of butadiene with ethylene". Journal of the American Chemical Society. 108 (3): 554–556. doi:10.1021/ja00263a059. PMID 22175504. 
    • Goldstein, E.; Beno, B.; Houk, K. N. (1996). "Density Functional Theory Prediction of the Relative Energies and Isotope Effects for the Concerted and Stepwise Mechanisms of the Diels−Alder Reaction of Butadiene and Ethylene". Journal of the American Chemical Society. 118 (25): 6036–6043. doi:10.1021/ja9601494. 
    • Breslow, R.; Guo, T. (1988). "Diels-Alder reactions in nonaqueous polar solvents. Kinetic effects of chaotropic and antichaotropic agents and of β-cyclodextrin". Journal of the American Chemical Society. 110 (17): 5613–5617. doi:10.1021/ja00225a003. 
    • Rideout, D. C.; Breslow, R. (1980). "Hydrophobic acceleration of Diels-Alder reactions". Journal of the American Chemical Society. 102 (26): 7816–7817. doi:10.1021/ja00546a048. 
    • Breslow, R.; Rizzo, C. J. (1991). "Chaotropic salt effects in a hydrophobically accelerated Diels-Alder reaction". Journal of the American Chemical Society. 113 (11): 4340–4341. doi:10.1021/ja00011a052. 
    • Blokzijl, Wilfried; Engberts, Jan B. F. N. (1992). "Initial-State and Transition-State Effects on Diels-Alder Reactions in Water and Mixed Aqueous Solvents". Journal of the American Chemical Society. 114 (13): 5440–5442. doi:10.1021/ja00039a074. 
    • Danishefsky, S.; Kitahara, T. (1974). "Useful diene for the Diels-Alder reaction". Journal of the American Chemical Society. 96 (25): 7807–7808. doi:10.1021/ja00832a031. 
    • Savard, J.; Brassard, P. (1979). "Regiospecific syntheses of quinones using vinylketene acetals derived from unsaturated esters". Tetrahedron Letters. 20 (51): 4911–4914. doi:10.1016/S0040-4039(01)86747-2. 
    • Kozmin, S. A.; Rawal, V. H. (1997). "Preparation and Diels−Alder Reactivity of 1-Amino-3-siloxy-1,3-butadienes". Journal of Organic Chemistry. 62 (16): 5252–5253. doi:10.1021/jo970438q. 
    • Klundt, I. L. (1970). "Benzocyclobutene and its derivatives". Chemical Reviews. 70 (4): 471–487. doi:10.1021/cr60266a002. 
    • Ito, Y.; Nakatsuka, M.; Saegusa, T. (1982). "Syntheses of polycyclic ring systems based on the new generation of o-quinodimethanes". Journal of the American Chemical Society. 104 (26): 7609–7622. doi:10.1021/ja00390a036. 
    • Sano, H.; Ohtsuka, H.; Migita, T. (1988). "A convenient method for the generation of o-quinodimethanes by proton induced 1,4-elimination of o-(1-hydroxyalkyl)benzyltributylstannanes". Journal of the American Chemical Society. 110 (6): 2014–2015. doi:10.1021/ja00214a083. 
    • Soon, H. W. (1993). "A novel method for the generation of o – quinodimethane by selenium – induced fragmentation of o – vinyl benzyltributylstannane". Tetrahedron Letters. 34 (47): 7587–7590. doi:10.1016/S0040-4039(00)60407-0. 
    • Soon, H. W. (1994). "Lewis acid-promoted generation of α-oxy-o-quinodimethanes and cycloaddition reactions". Tetrahedron Letters. 35 (23): 3975–3978. doi:10.1016/S0040-4039(00)76717-7. 
    • Rubottom, G. M.; Way, J. E. (1984). "An Improved Method for the Preparation of o-Quinodimethanes". Synthetic Communications. 14 (6): 507–514. doi:10.1080/00397918408059572. 
    • Ranganathan, S.; Ranganathan, D.; Mehrotra, A. K. (1977). "Ketene Equivalents". Synthesis. 1977 (5): 289–296. doi:10.1055/s-1977-24362. 

nih.gov

ncbi.nlm.nih.gov

  • Dewar, M. J.; Olivella, S.; Stewart, J. J. (1986). "Mechanism of the Diels-Alder reaction: Reactions of butadiene with ethylene and cyanoethylenes". Journal of the American Chemical Society. 108 (19): 5771–5779. doi:10.1021/ja00279a018. PMID 22175326. 
  • Houk, K. N.; Lin, Y. T.; Brown, F. K. (1986). "Evidence for the concerted mechanism of the Diels-Alder reaction of butadiene with ethylene". Journal of the American Chemical Society. 108 (3): 554–556. doi:10.1021/ja00263a059. PMID 22175504. 

nobelprize.org

worldcat.org