Zobrazeno 1 - 10
of 171
pro vyhledávání: '"Susan E. Gibson"'
Autor:
Susan E. Gibson
Publikováno v:
Digital Studies, Vol 0, Iss 9 (2009)
None
Externí odkaz:
https://doaj.org/article/d0649842bacd442d84acc3e9f6d30b53
Autor:
Susan E. Gibson
Do you want to travel and make a positive impact on the world? This book is designed for you.How to Be an Amazing Volunteer Overseas will give you essential advice on how to decide what to do and where to go. It will help you to prepare for life in a
Autor:
Frank Prechtl, Adam T. Wierzchleyski, Susan E. Gibson, Paul W. N. Christian, Richard Gil, Carlos F. Marcos, P. Caroline V. Jones
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 114:195-202
Tricarbonylchromium(0) complexes of sulfur, phosphorus, silicon, iodine, tin and carbon substituted (S)-(α-methylbenzyl)dimethylamines are oxidized by dimethyldioxirane to enantiomerically pure tricarbonylchromium(0) complexes of substituted styrene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77e584ebb29f71d3ecaeedd675778c59
https://doi.org/10.1002/recl.19951140411
https://doi.org/10.1002/recl.19951140411
Autor:
Keren Abecassis, Susan E. Gibson
Publikováno v:
European Journal of Organic Chemistry. 2010:2938-2944
The first enantioselective synthesis of gossonorol has been achieved in good overall yield and excellent enantioselectivity, demonstrating the utility of a novel approach to enantiopure tertiary benzylic alcohols. Epoxidation of enantiopure gossonoro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a40a7a6dd5b4845156fe55754de1289
https://doi.org/10.1002/ejoc.201000391
https://doi.org/10.1002/ejoc.201000391
Publikováno v:
Tetrahedron. 65:7498-7503
A new synthetic route to the bisphosphonate enyne tetraethyl hept-1-yn-6-en-4,4-diylbisphosphonate has been developed and the enyne has been used successfully in a range of transition metal-catalysed cyclisations that give structurally varied product
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8274b775f6fb0d531ab073f9d64d933
https://doi.org/10.1016/j.tet.2009.07.007
https://doi.org/10.1016/j.tet.2009.07.007
Publikováno v:
European Journal of Organic Chemistry. 2009:1606-1611
Allyl ethers of the tricarbonylchromium(0) complexes of benzylic alcohols undergo highly enantioselective benzylic functionalisation using a chiral base/electrophilic quench sequence; the allyl group is readily removed to reveal a hydroxy group as de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d9047f7c7fac5d93c39fe811c10ca5d
https://doi.org/10.1002/ejoc.200900007
https://doi.org/10.1002/ejoc.200900007
Publikováno v:
European Journal of Organic Chemistry. 2008:4963-4971
The stereocontrolled synthesis of enantiomeric pairs of four ethers, in which the oxygen atom is flanked by two αstereocentres, has been achieved using a chiral base/arene chromium tricarbonyl activation approach. (© Wiley-VCH Verlag GmbH & Co. KGa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ffdae89032501ec10b551d3e8f43fcc
https://doi.org/10.1002/ejoc.200800634
https://doi.org/10.1002/ejoc.200800634
Synthesis and CD spectroscopy of polyethers with homochiral and heterochiral layers of stereocentres
Publikováno v:
Tetrahedron. 64:6615-6627
Eight polyethers with three to nine stereocentres have been synthesised using chiral base methodology. Examination of the polyethers by CD spectroscopy revealed clear differences between homochiral isomers and isomers with a heterochiral relationship
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::307f43b94e8538ab3a2f207e7e57d16a
https://doi.org/10.1016/j.tet.2008.05.028
https://doi.org/10.1016/j.tet.2008.05.028
Publikováno v:
Pure and Applied Chemistry. 80:903-911
A study of the Pauson-Khand reaction (PKR) based on Co2(CO)8 and binap has revealed that a key precatalyst is (binap)Co2(CO)6, and that alkynes add to this species to generate isomers that interconvert under typical PKR conditions. A 31P NMR study of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a873170d2a79b1549d927cbf837f152d
https://doi.org/10.1351/pac200880050903
https://doi.org/10.1351/pac200880050903
Autor:
Jacob T. Rendell, Susan E. Gibson
Publikováno v:
Chem. Commun.. :922-941
This review highlights important developments in the pursuit of chiral conformational order in dendritic structures. To be able to create and control chiral secondary structure necessitates a thorough understanding of how chiral subunits influence th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93f53b8eef23f6e6e0c28aee0e6be685
https://doi.org/10.1039/b712298e
https://doi.org/10.1039/b712298e