Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Graham M. Kyne"'
Autor:
Khalil A. Abboud, Nathalie L'Helias, Peter Schmidt, Graham M. Kyne, Marie E. Krafft, Chitaru Hirosawa
Publikováno v:
Tetrahedron. 62:11782-11792
Tricyclic skeletons have been generated from acyclic enyne precursors by using an intramolecular Pauson–Khand reaction in combination with aldol, Michael and alkylation reactions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::040aedcf06df9f15d56136bc7b3d345c
https://doi.org/10.1016/j.tet.2006.09.022
https://doi.org/10.1016/j.tet.2006.09.022
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :841-864
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e90af714b85f1b0c33c95cc29a37bbd
https://doi.org/10.1039/b009041g
https://doi.org/10.1039/b009041g
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1258-1263
A series of acyclic thiourea derivatives, designed to create a cleft with four hydrogen bond donors suitable for carboxylate recognition, have been prepared, and their ability to bind to N-protected amino acid carboxylate salts has been investigated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c13bc8327d873a8b7b197d0b777ccb7e
https://doi.org/10.1039/b102298a
https://doi.org/10.1039/b102298a
Publikováno v:
Angewandte Chemie. 114:4407-4409
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21932c2634eb0bd3a7baa6ededa9246d
https://doi.org/10.1002/1521-3757(20021115)114:22<4407::aid-ange4407>3.0.co
https://doi.org/10.1002/1521-3757(20021115)114:22<4407::aid-ange4407>3.0.co
Publikováno v:
ChemInform. 32
A series of acyclic thiourea derivatives, designed to create a cleft with four hydrogen bond donors suitable for carboxylate recognition, have been prepared, and their ability to bind to N-protected amino acid carboxylate salts has been investigated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1c9494146a0319c7b5708f9e885fa6e
https://doi.org/10.1002/chin.200143203
https://doi.org/10.1002/chin.200143203
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::188f13fffb3afdc046011d10a5febcb2
https://doi.org/10.1002/chin.200231260
https://doi.org/10.1002/chin.200231260
Publikováno v:
Angewandte Chemie (International ed. in English). 41(22)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2f9c5b899a0a693bc211117b374478c5
https://pubmed.ncbi.nlm.nih.gov/12434348
https://pubmed.ncbi.nlm.nih.gov/12434348
Publikováno v:
ResearcherID
The development of enantioselective receptors continues to be a challenging endeavor for supramolecular chemists, and enantioselective recognition of biologically relevant molecules in competitive solvents is particularly demanding.[1] Although numer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79765a1bc188069606322cb2cf3be209
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000179506300007&KeyUID=WOS:000179506300007
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000179506300007&KeyUID=WOS:000179506300007
