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4+4 Photocycloaddition (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "4+4 Photocycloaddition" in English language version.

refsWebsite
Global rank English rank
10doi.org
2nd place
2nd place
3nih.gov
4th place
4th place
1semanticscholar.org
11th place
8th place

doi.org

  • Fieser, Louis F.; Lothrop, Warren C. (1936). "The Structure of Anthracene". J. Am. Chem. Soc. 58 (5): 749–753. doi:10.1021/ja01296a016.
  • Heiko, I.; Luo, J. (2008). "The reversible [4 + 4] photocycloaddition of acridizinium derivatives". J. Photochem. Photobiol. A. 200: 3–9. doi:10.1016/j.jphotochem.2008.04.008.
  • Zhu, M.; Qiu, Z.; Hiel, G.; Sieburth, S. (2002). "Photocycloaddition of Four-Carbon-Tethered Pyridones. Intramolecular Hydrogen Bonding and Facilitated Amide Hydrolysis by a Proximal Secondary Alcohol". J. Org. Chem. 67 (10): 3487–3493. doi:10.1021/jo025565n. PMID 12003564.
  • Wender, P.; Smith, T. (1998). "Transition Metal-Catalyzed Intramolecular [4+2] Cycloadditions: Mechanistic and Synthetic Investigations". Tetrahedron. 54 (7): 1255–1275. doi:10.1016/S0040-4020(97)10223-X.
  • Lei, L.; Benderb, J.; West F. G. (2009). "Diastereocontrol in [4+4]-photocycloadditions of pyran-2-ones: effect of ring substituents and chiral ketal". Tetrahedron Lett. 50 (11): 1188–1192. doi:10.1016/j.tetlet.2008.12.117.
  • Song, D.; McDonald, R.; West, F. G. (2006). "Diastereoselective [4 + 4]-photocycloaddition reactions of pyran-2-ones: rapid access to functionalized 5-8-5 skeletons". Org. Lett. 8 (18): 4075–4078. doi:10.1021/ol061576h. PMID 16928077.
  • Lee, Y.-G.; McGee, K. F.; Chen, J.; Rucando, D.; Sieburth, S. McN. (2000). "A [4 + 4] 2-Pyridone Approach to Taxol. 3. Stereocontrol during Elaboration of the Cyclooctane". J. Org. Chem. 65 (20): 6676–6681. doi:10.1021/jo005532c. PMID 11052118.
  • McGee, K. F.; Al-Tel, T. H.; Sieburth, S. McN. (2001). "Fusicoccin Synthesis by Intramolecular [4+4] Photocycloaddition of 2-Pyridones: Stereocontrol of the Cycloaddition and Elaboration of the Pentacyclic Product". Synthesis. 112 (8): 1185–1196. doi:10.1055/s-2001-15066. S2CID 95258628.
  • Sieburth, S. McN.; Al-Tel, T. H.; Rucando, D. (1997). "Beyond the medium ring: A [4 + 4] Cycloaddition/Fragmentation Synthesis of Eleven-membered Rings". Tetrahedron Lett. 38 (49): 8433–8434. doi:10.1016/S0040-4039(97)10272-6.
  • Sieburth, S. McN.; Cunard, N. T. (1996). "The [4 + 4] cycloaddition and its strategic application in natural product synthesis". Tetrahedron. 52 (18): 6251–6282. doi:10.1016/0040-4020(95)01077-7.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Zhu, M.; Qiu, Z.; Hiel, G.; Sieburth, S. (2002). "Photocycloaddition of Four-Carbon-Tethered Pyridones. Intramolecular Hydrogen Bonding and Facilitated Amide Hydrolysis by a Proximal Secondary Alcohol". J. Org. Chem. 67 (10): 3487–3493. doi:10.1021/jo025565n. PMID 12003564.
  • Song, D.; McDonald, R.; West, F. G. (2006). "Diastereoselective [4 + 4]-photocycloaddition reactions of pyran-2-ones: rapid access to functionalized 5-8-5 skeletons". Org. Lett. 8 (18): 4075–4078. doi:10.1021/ol061576h. PMID 16928077.
  • Lee, Y.-G.; McGee, K. F.; Chen, J.; Rucando, D.; Sieburth, S. McN. (2000). "A [4 + 4] 2-Pyridone Approach to Taxol. 3. Stereocontrol during Elaboration of the Cyclooctane". J. Org. Chem. 65 (20): 6676–6681. doi:10.1021/jo005532c. PMID 11052118.

semanticscholar.org

api.semanticscholar.org

  • McGee, K. F.; Al-Tel, T. H.; Sieburth, S. McN. (2001). "Fusicoccin Synthesis by Intramolecular [4+4] Photocycloaddition of 2-Pyridones: Stereocontrol of the Cycloaddition and Elaboration of the Pentacyclic Product". Synthesis. 112 (8): 1185–1196. doi:10.1055/s-2001-15066. S2CID 95258628.