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Poingdestre, Sarah-Jane, Goodacre, Jonathan D., Weller, Andrew S., Willis, Michael C. (2012) Rhodium-catalysed linear-selective alkyne hydroacylation. Chemical Communications, 48 (51). 6354pp. doi:10.1039/c2cc32713a

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Reference TypeJournal (article/letter/editorial)
TitleRhodium-catalysed linear-selective alkyne hydroacylation
JournalChemical Communications
AuthorsPoingdestre, Sarah-JaneAuthor
Goodacre, Jonathan D.Author
Weller, Andrew S.Author
Willis, Michael C.Author
Year2012Volume48
Issue51
PublisherRoyal Society of Chemistry (RSC)
DOIdoi:10.1039/c2cc32713aSearch in ResearchGate
Generate Citation Formats
Mindat Ref. ID8141504Long-form Identifiermindat:1:5:8141504:7
GUID0
Full ReferencePoingdestre, Sarah-Jane, Goodacre, Jonathan D., Weller, Andrew S., Willis, Michael C. (2012) Rhodium-catalysed linear-selective alkyne hydroacylation. Chemical Communications, 48 (51). 6354pp. doi:10.1039/c2cc32713a
Plain TextPoingdestre, Sarah-Jane, Goodacre, Jonathan D., Weller, Andrew S., Willis, Michael C. (2012) Rhodium-catalysed linear-selective alkyne hydroacylation. Chemical Communications, 48 (51). 6354pp. doi:10.1039/c2cc32713a
In(2012) Chemical Communications Vol. 48 (51) Royal Society of Chemistry (RSC)

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Hooper, Joel F., Young, Rowan D., Weller, Andrew S., Willis, Michael C. (2013) Traceless Chelation-Controlled Rhodium-Catalyzed Intermolecular Alkene and Alkyne Hydroacylation. Chemistry - A European Journal, 19 (9). 3125-3130 doi:10.1002/chem.201204056
González-Rodríguez, Carlos, Pawley, Rebekah J., Chaplin, Adrian B., Thompson, Amber L., Weller, Andrew S., Willis, Michael C. (2011) Rhodium-Catalyzed Branched-Selective Alkyne Hydroacylation: A Ligand-Controlled Regioselectivity Switch. Angewandte Chemie, 123 (22). 5240-5244 doi:10.1002/ange.201100956
González-Rodríguez, Carlos, Pawley, Rebekah J., Chaplin, Adrian B., Thompson, Amber L., Weller, Andrew S., Willis, Michael C. (2011) Rhodium-Catalyzed Branched-Selective Alkyne Hydroacylation: A Ligand-Controlled Regioselectivity Switch. Angewandte Chemie International Edition, 50 (22). 5134-5138 doi:10.1002/anie.201100956
Neuhaus, James D., Morrow, Sarah M., Brunavs, Michael, Willis, Michael C. (2016) Diversely Substituted Quinolines via Rhodium-Catalyzed Alkyne Hydroacylation. Organic Letters, 18. 1562-1565 doi:10.1021/acs.orglett.6b00390
Neuhaus, James D., Morrow, Sarah M., Brunavs, Michael, Willis, Michael C. (2016) Correction to “Diversely Substituted Quinolines via Rhodium-Catalyzed Alkyne Hydroacylation”. Organic Letters, 18. 2519 doi:10.1021/acs.orglett.6b01218
Chaplin, Adrian B., Hooper, Joel F., Weller, Andrew S., Willis, Michael C. (2012) Intermolecular Hydroacylation: High Activity Rhodium Catalysts Containing Small-Bite-Angle Diphosphine Ligands. Journal Of The American Chemical Society, 134 (10) 4885-4897 doi:10.1021/ja211649a
Coxon, Thomas J., Fernández, Maitane, Barwick-Silk, James, McKay, Alasdair I., Britton, Louisa E., Weller, Andrew S., Willis, Michael C. (2017) Exploiting Carbonyl Groups to Control Intermolecular Rhodium-Catalyzed Alkene and Alkyne Hydroacylation. Journal Of The American Chemical Society, 139 (29) 10142-10149 doi:10.1021/jacs.7b05713
Pawley, Rebekah J., Huertos, Miguel A., Lloyd-Jones, Guy C., Weller, Andrew S., Willis, Michael C. (2012) Intermolecular Alkyne Hydroacylation. Mechanistic Insight from the Isolation of the Vinyl Intermediate That Precedes Reductive Elimination. Organometallics, 31. 5650-5659 doi:10.1021/om300647n
Moseley, Daniel F., Kalepu, Jagadeesh, Willis, Michael C. (2021) Azine-N-oxides as effective controlling groups for Rh-catalysed intermolecular alkyne hydroacylation. Chemical Science, 12 (39) 13068-13073 doi:10.1039/d1sc03915f
Straker, Robert N., Majhail, Manjeet K., Willis, Michael C. (2017) Exploiting rhodium-catalysed ynamide hydroacylation as a platform for divergent heterocycle synthesis. Chemical Science, 8. 7963-7968 doi:10.1039/c7sc03795c
Huertos, Miguel A., Weller, Andrew S. (2012) Intermediates in the Rh-catalysed dehydrocoupling of phosphine–borane. Chemical Communications, 48 (57). 7185pp. doi:10.1039/c2cc32696e
 
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