Sign In

Login

Password

Forgot Password ? Sign Up

Azomethine ylide (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Azomethine ylide" in English language version.

refsWebsite
Global rank English rank
23doi.org
2nd place
2nd place
13nih.gov
4th place
4th place
1rsc.org
2,020th place
1,872nd place
1semanticscholar.org
11th place
8th place

doi.org

  • Coldham, Iain; Hufton, Richard (2005). "Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides". Chemical Reviews. 105 (7): 2765–2809. doi:10.1021/cr040004c. PMID 16011324.
  • Padwa, Albert; Pearson, William H.; Harwood, L. M.; Vickers, R. J. (2003). "Chapter 3. Azomethine Ylides". Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products. Chemistry of Heterocyclic Compounds: A Series of Monographs. Vol. 59. pp. 169–252. doi:10.1002/0471221902.ch3. ISBN 9780471387268.
  • Adrio, Javier; Carretero, Juan C. (2011). "Novel dipolarophiles and dipoles in the metal-catalyzed enantioselective 1,3-dipolar cycloaddition of azomethine ylides". Chemical Communications. 47 (24): 6784–6794. doi:10.1039/c1cc10779h. PMID 21472157.
  • Dauban, Philippe; Guillaume, Malik (2009). "A Masked 1,3-Dipole Revealed from Aziridines". Angewandte Chemie International Edition. 48 (48): 9026–9029. doi:10.1002/anie.200904941. PMID 19882612.
  • Huisgen, Rolf; Scheer, Wolfgang; Huber, Helmut (1967). "Stereospecific Conversion of cis-trans Isomeric Aziridines to Open-Chain Azomethine Ylides". Journal of the American Chemical Society. 89 (7): 1753–1755. doi:10.1021/ja00983a052.
  • Banks, Harold D. (2010). "Torquoselectivity Studies in the Generation of Azomethine Ylides from Substituted Aziridines". Journal of Organic Chemistry. 75 (8): 2510–2517. doi:10.1021/jo902600y. PMID 20329779.
  • Cardoso, Ana L.; Pinho e Melo, Teresa M. V. D. (2012). "Aziridines in Formal [3+2]Cycloadditions: Synthesis of Five-Membered Heterocycles". European Journal of Organic Chemistry (33): 6479–6501. doi:10.1002/ejoc.201200406.
  • Huie, Edward (1983). "Intramolecular [3+2]cycloaddition routes to carbon-bridged dibenzocycloheptanes and dibenzazepines". Journal of Organic Chemistry. 48 (18): 2994–2997. doi:10.1021/jo00166a011.
  • Padwa, Albert; Gingrich, Henry L.; Lim, Richard (1982). "Regiochemistry of intramolecular munchnone cycloadditions: preparative and mechanistic implications". Journal of Organic Chemistry. 47 (12): 2447–2456. doi:10.1021/jo00133a041.
  • Li, Yi; Houk, Kendall N.; González, Javier (1995). "Pericyclic Reaction Transition States". Accounts of Chemical Research. 20 (2): 81–90. doi:10.1021/ar00050a004.
  • Heathcock, Clayton H.; Henke, Brad R.; Kouklis, Andrew J. (1992). "Intramolecular 1,3-Dipolar Cycloaddition of Stabilized Azomethine Ylides to Unactivated Dipolarophiles". Journal of Organic Chemistry. 57 (56): 7056–7066. doi:10.1021/jo00052a015.
  • Streiber, S. L. (2003). "Catalytic asymmetric [3+2]cycloaddition of azomethine ylides. Development of a versatile stepwise, three-component reaction for diversity-oriented synthesis". Journal of the American Chemical Society. 125 (34): 10174–10175. doi:10.1021/ja036558z. PMID 12926931.
  • Adrio, Javier; Carreter, Juan C. (2011). "Novel dipolarophiles and dipoles in the metal-catalyzed enantioselective 1,3-dipolar cycloaddition of azomethine ylides". Chemical Communications. 47 (24): 6784–6794. doi:10.1039/c1cc10779h. PMID 21472157.
  • Zhang, Xumu; Raghunath, Malati; Gao, Wenzhong (2005). "Cu(I)-Catalyzed Highly Exo-selective and Enantioselective [3+2]Cycloaddition of Azomethine Ylides with Acrylates". Organic Letters. 7 (19): 4241–4244. doi:10.1021/ol0516925. PMID 16146397.
  • Fukuzawa, Shin-ichi; Oura, Ichiro; Shimizu, Kenta; Ogata, Kenichi (2010). "Highly Endo-Selective and Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylide with α-Enones Catalyzed by a Silver(I)/ThioClickFerrophos Complex". Organic Letters. 12 (8): 1752–1755. doi:10.1021/ol100336q. PMID 20232852.
  • Allway, Philip; Grigg, Ronald (1991). "Chiral cobalt(II) and manganese(II) catalysts for the 1,3-dipolar cycloaddition reactions of azomethine ylides derived from arylidene imines of glycine". Tetrahedron Letters. 32 (41): 5817–5820. doi:10.1016/S0040-4039(00)93563-9.
  • Gong, Liu-Zhu; Chen, Xiao-Hua; Wei, Qiang; Luo, Shi-Wei; Xiao, Han (2009). "Organocatalytic Synthesis of Spiro[pyrrolidin-3,3′-oxindoles] with High Enantiopurity and Structural Diversity". Journal of the American Chemical Society. 131 (38): 13819–13825. doi:10.1021/ja905302f. PMID 19736987.
  • Nedolya, N. A.; Trofimov, B. A. (2013). "[1,7]-Electrocyclization reactions in the synthesis of azepine derivatives". Chemistry of Heterocyclic Compounds. 49 (1): 152–176. doi:10.1007/s10593-013-1236-y. S2CID 96192354.
  • Nyerges, Miklós (2006). "1,7-Electrocyclization reactions of stabilized α,β:γ,δ-unsaturated azomethine ylides". Tetrahedron. 16 (24): 5725–5735. doi:10.1016/j.tet.2006.03.088.
  • Nierengarten, Jean-François (2002). "An unexpected Diels–Alder reaction on the fullerene core rather than an expected 1,3-dipolar cycloaddition". Chem. Commun. (7): 712–713. doi:10.1039/B201122K. PMID 12119686.
  • Snider, B. B.; Ahn, Y.; O'Hare, S. M. (2001). "Total synthesis of (±)-martinellic acid". Organic Letters. 3 (26): 4217–4220. doi:10.1021/ol016884o. PMID 11784181.
  • Williams, Robert (2003). "Concise, Asymmetric Total Synthesis of Spirotryprostatin A". Organic Letters. 5 (17): 3135–3137. doi:10.1021/ol0351910. PMID 12917000.
  • Ryan, John H. (2011). "1,3-Dipolar cycloaddition-decarboxylation reactions of an azomethine ylide with isatoic anhydrides: formation of novel benzodiazepinones". Organic Letters. 13 (3): 486–489. doi:10.1021/ol102824k. PMID 21175141.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Coldham, Iain; Hufton, Richard (2005). "Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides". Chemical Reviews. 105 (7): 2765–2809. doi:10.1021/cr040004c. PMID 16011324.
  • Adrio, Javier; Carretero, Juan C. (2011). "Novel dipolarophiles and dipoles in the metal-catalyzed enantioselective 1,3-dipolar cycloaddition of azomethine ylides". Chemical Communications. 47 (24): 6784–6794. doi:10.1039/c1cc10779h. PMID 21472157.
  • Dauban, Philippe; Guillaume, Malik (2009). "A Masked 1,3-Dipole Revealed from Aziridines". Angewandte Chemie International Edition. 48 (48): 9026–9029. doi:10.1002/anie.200904941. PMID 19882612.
  • Banks, Harold D. (2010). "Torquoselectivity Studies in the Generation of Azomethine Ylides from Substituted Aziridines". Journal of Organic Chemistry. 75 (8): 2510–2517. doi:10.1021/jo902600y. PMID 20329779.
  • Streiber, S. L. (2003). "Catalytic asymmetric [3+2]cycloaddition of azomethine ylides. Development of a versatile stepwise, three-component reaction for diversity-oriented synthesis". Journal of the American Chemical Society. 125 (34): 10174–10175. doi:10.1021/ja036558z. PMID 12926931.
  • Adrio, Javier; Carreter, Juan C. (2011). "Novel dipolarophiles and dipoles in the metal-catalyzed enantioselective 1,3-dipolar cycloaddition of azomethine ylides". Chemical Communications. 47 (24): 6784–6794. doi:10.1039/c1cc10779h. PMID 21472157.
  • Zhang, Xumu; Raghunath, Malati; Gao, Wenzhong (2005). "Cu(I)-Catalyzed Highly Exo-selective and Enantioselective [3+2]Cycloaddition of Azomethine Ylides with Acrylates". Organic Letters. 7 (19): 4241–4244. doi:10.1021/ol0516925. PMID 16146397.
  • Fukuzawa, Shin-ichi; Oura, Ichiro; Shimizu, Kenta; Ogata, Kenichi (2010). "Highly Endo-Selective and Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylide with α-Enones Catalyzed by a Silver(I)/ThioClickFerrophos Complex". Organic Letters. 12 (8): 1752–1755. doi:10.1021/ol100336q. PMID 20232852.
  • Gong, Liu-Zhu; Chen, Xiao-Hua; Wei, Qiang; Luo, Shi-Wei; Xiao, Han (2009). "Organocatalytic Synthesis of Spiro[pyrrolidin-3,3′-oxindoles] with High Enantiopurity and Structural Diversity". Journal of the American Chemical Society. 131 (38): 13819–13825. doi:10.1021/ja905302f. PMID 19736987.
  • Nierengarten, Jean-François (2002). "An unexpected Diels–Alder reaction on the fullerene core rather than an expected 1,3-dipolar cycloaddition". Chem. Commun. (7): 712–713. doi:10.1039/B201122K. PMID 12119686.
  • Snider, B. B.; Ahn, Y.; O'Hare, S. M. (2001). "Total synthesis of (±)-martinellic acid". Organic Letters. 3 (26): 4217–4220. doi:10.1021/ol016884o. PMID 11784181.
  • Williams, Robert (2003). "Concise, Asymmetric Total Synthesis of Spirotryprostatin A". Organic Letters. 5 (17): 3135–3137. doi:10.1021/ol0351910. PMID 12917000.
  • Ryan, John H. (2011). "1,3-Dipolar cycloaddition-decarboxylation reactions of an azomethine ylide with isatoic anhydrides: formation of novel benzodiazepinones". Organic Letters. 13 (3): 486–489. doi:10.1021/ol102824k. PMID 21175141.

rsc.org

pubs.rsc.org

  • R. Berger, M. Wagner, X. Feng, K. Müllen. “Polycyclic aromatic azomethine ylides: a unique entry to extended polycyclic heteroaromatics”. 2014. 436–441.doi: 10.1039/C4SC02793K

semanticscholar.org

api.semanticscholar.org

  • Nedolya, N. A.; Trofimov, B. A. (2013). "[1,7]-Electrocyclization reactions in the synthesis of azepine derivatives". Chemistry of Heterocyclic Compounds. 49 (1): 152–176. doi:10.1007/s10593-013-1236-y. S2CID 96192354.