Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Arife, Yazici"'
Autor:
Thanphat Thaima, Stephen G. Pyne, Thunwadee Limtharakul, Anthony C. Willis, Chiramet Auranwiwat, Uta Wille, Arife Yazici
Publikováno v:
Organic & Biomolecular Chemistry. 19:259-272
The reactions of α,β-unsaturated N-acyliminium ions, generated in situ from 4(S)-O-substitutedhydroxy-5-hydroxy-5-vinyl-N-alkylpyrrolidin-2-ones, with allylsilanes and indoles leading to the formation of spirocyclic heterocycles, are reported. Six
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cd7a2dd426e72d1eb20abfcd6e42290
https://doi.org/10.1039/d0ob02075c
https://doi.org/10.1039/d0ob02075c
Autor:
Thanphat, Thaima, Arife, Yazici, Chiramet, Auranwiwat, Anthony C, Willis, Uta, Wille, Thunwadee, Limtharakul, Stephen G, Pyne
Publikováno v:
Organicbiomolecular chemistry. 19(1)
The reactions of α,β-unsaturated N-acyliminium ions, generated in situ from 4(S)-O-substitutedhydroxy-5-hydroxy-5-vinyl-N-alkylpyrrolidin-2-ones, with allylsilanes and indoles leading to the formation of spirocyclic heterocycles, are reported. Six
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f2e89b235fe3c7051d4efe5891269ee7
https://pubmed.ncbi.nlm.nih.gov/33191414
https://pubmed.ncbi.nlm.nih.gov/33191414
Publikováno v:
ChemInform. 47
Novel tricyclic bridged heterocyclic systems can be readily prepared from sequential 1,4- and 1,2-addition reactions of allyl and 3-substituted allylsilanes to indolizidine and quinolizidine α,β-unsaturated N-acyliminium ions. These reactions invol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5224707e85cf7fbf02d65098eb5c6bc7
https://doi.org/10.1002/chin.201627121
https://doi.org/10.1002/chin.201627121
Publikováno v:
The Journal of organic chemistry. 81(4)
Novel tricyclic bridged heterocyclic systems can be readily prepared from sequential 1,4- and 1,2-addition reactions of allyl and 3-substituted allylsilanes to indolizidine and quinolizidine α,β-unsaturated N-acyliminium ions. These reactions invol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac3b21bcd1a7963826936f62aeaedec6
https://pubmed.ncbi.nlm.nih.gov/26816207
https://pubmed.ncbi.nlm.nih.gov/26816207
Publikováno v:
The Journal of Organic Chemistry. 75:3412-3419
The CuX (X = I, Br, Cl, CN)-mediated cyclization-halogenation and cyclization-cyanation reactions of beta-hydroxyalkynes and o-alkynylphenol and -aniline derivatives give rise to 3-halo- and 3-cyanofuro[3,2-b]pyrroles, 3-iodo-, 3-bromo-, and 3-cyanob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18eb6d7add5311e9b1c84ea47cc241ed
https://doi.org/10.1021/jo1005119
https://doi.org/10.1021/jo1005119
Autor:
Jasmine C, Jury, Nalivela Kumara, Swamy, Arife, Yazici, Ian R, Morgan, Anthony C, Willis, Stephen G, Pyne
Publikováno v:
The Journal of Organic Chemistry. 74:5523-5527
Furo[3,2-b]pyrroles and furo[3,2-b]pyridines can be conveniently prepared in good yields from the cycloisomerization reactions of cis-4-hydroxy-5-alkynylpyrrolidinones and cis-5-hydroxy-6-alkynylpiperidinones, respectively, using Ag(I), Pd(II)/Cu(I),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e99c18cbd877b7359885e55c9ba90768
https://doi.org/10.1021/jo9007942
https://doi.org/10.1021/jo9007942
Autor:
Arife Yazici, Stephen G. Pyne
Publikováno v:
Synthesis. 2009:513-541
This review highlights the advances in the literature up to July2008 on the intermolecular reactions of acyclic and cyclic N-acyliminium ions. This is an updateof an earlier review in 2000 on this topic and does not includeintramolecular addition rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5de47d003eef4c2a70a1df69be517059
https://doi.org/10.1055/s-0028-1083346
https://doi.org/10.1055/s-0028-1083346
Publikováno v:
Tetrahedron. 64:1409-1419
The addition of boronic acids to five- and six-membered ring N-acyliminium ions has been employed to prepare 5- and 6-substituted 4-hydroxypyrrolidin-2-ones and 5-hydroxypiperidin-2-ones, respectively, in a diastereoselective fashion.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20a8173d9cf02b568ce65e4ef8cf410c
https://doi.org/10.1016/j.tet.2007.11.046
https://doi.org/10.1016/j.tet.2007.11.046
Autor:
Thunwadee Ritthiwigrom, Andrew S. Davis, Stephen G. Pyne, Arife Yazici, Christopher W. G. Au, Ian Rhys Morgan
Publikováno v:
Pure and Applied Chemistry. 80:751-762
We have demonstrated that the borono-Mannich reaction is a versatile and efficient reaction for the diastereoselective preparation of chiral 1,2-amino alcohols. These Mannich products are valuable starting materials as shown in this report by the syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43d4d4a03fd79862852e03cd9ac9ae9f
https://doi.org/10.1351/pac200880040751
https://doi.org/10.1351/pac200880040751
Autor:
Stephen G. Pyne, Arife Yazici
Publikováno v:
Tetrahedron Letters. 52:1398-1400
The Cu(I) halide (X = I, Br, Cl) mediated reactions of Cbz-protected cis -2-phenylethenyl-3-hydroxypyrrolidine gave novel 3-halo-2,5-trisubstituted furans in good yields, via a cyclization-halogenation, ring-opening reaction sequence. In contrast, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e476ce25fbf183af88ee4cc1dd005f91
https://doi.org/10.1016/j.tetlet.2011.01.120
https://doi.org/10.1016/j.tetlet.2011.01.120