Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Whitehead Andrew Jonathan"'
Publikováno v:
Synlett. 2008:2097-2100
6 -Oxohexa-2,3-dienoates can be readily prepared via an atom economical Claisen rearrangement of propargyl vinyl ethers formed in situ by the reaction of propargylic alcohols with acetals. Preliminary experiments have demonstrated that these function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7cbcf8aa0fc5ac52771f707284aabc04
https://doi.org/10.1055/s-2008-1078028
https://doi.org/10.1055/s-2008-1078028
Publikováno v:
Synlett. 2007:0431-0434
The selection of electron-deficient allenes as substrates for highly regioselective vinylogous amide formation leads to a convenient one-pot [3+3] annulation sequence for the construction of highly functionalized cyclic enamides. By the selection of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dff75b91259def00b030abaaf0b569ba
https://doi.org/10.1055/s-2007-967955
https://doi.org/10.1055/s-2007-967955
Publikováno v:
Synlett. :0805-0808
Reaction of 2-hydroxy-3-butenoates with a series of carbonyl derivatives gives substituted 6-oxo-2-hexenoates in good yields under mild acid conditions via Claisen rearrangement of the allyl alkenyl ether intermediate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb396e3ed3ae22b886e83715ffee4c84
https://doi.org/10.1055/s-2003-38732
https://doi.org/10.1055/s-2003-38732
Autor:
Whitehead Andrew Jonathan, Catherine Mills, Alexander McKillop, David F. Emiabata-Smith, William B. Motherwell
Publikováno v:
Synlett. 2001:1302-1304
A rhodium(I)-catalysed tandem hydrosilylation-intramolecular aldol sequence can be used to prepare substituted cycloalkanols in modest to excellent yields under mild reaction conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4949d1c0c55e827992ff678a095e0678
https://doi.org/10.1055/s-2001-16044
https://doi.org/10.1055/s-2001-16044
Autor:
Michael David Goodyear, Whitehead Andrew Jonathan, Latham William David Stuart, Mark J. Coleman
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17ddbb2e8b129f8bbf77c7cb75fa8207
https://doi.org/10.1002/chin.200012095
https://doi.org/10.1002/chin.200012095
Publikováno v:
ChemInform. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15fec4eaaeb9ba691ff6a725adfe4357
https://doi.org/10.1002/chin.200852058
https://doi.org/10.1002/chin.200852058
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cd5d248cfb1da562480cc6b2b2bd665
https://doi.org/10.1002/chin.200428050
https://doi.org/10.1002/chin.200428050
Publikováno v:
ChemInform. 34
Reaction of 2-hydroxy-3-butenoates with a series of carbonyl derivatives gives substituted 6-oxo-2-hexenoates in good yields under mild acid conditions via Claisen rearrangement of the allyl alkenyl ether intermediate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d02d65503abce30bc8601df9a5f4897
https://doi.org/10.1002/chin.200333082
https://doi.org/10.1002/chin.200333082
Autor:
Latham William David Stuart, Whitehead Andrew Jonathan, Mark J. Coleman, Michael David Goodyear
Publikováno v:
Synlett. 1999:1923-1924
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b27096d30f382236f64edd8975df04b
https://doi.org/10.1055/s-1999-2978
https://doi.org/10.1055/s-1999-2978