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pro vyhledávání: '"Carly J. Mueller"'
Autor:
Carly J. Mueller, Ana M. Neferu, C. Wade Downey, Stephanie Corsi, Smaranda Craciun, Christina A. Vivelo
Publikováno v:
Tetrahedron Letters. 53:5766-5768
Ethyl propiolate undergoes one-pot three-step thioconjugate addition-oxidation-Diels–Alder cycloaddition when treated with a variety of thiols in the presence of catalytic base, meta-chloroperbenzoic acid, lithium perchlorate, and cyclopentadiene.
Autor:
Christina A. Vivelo, Eric W. Etchill, Ryan J. Sault, Carly J. Mueller, C. Wade Downey, Ana M. Neferu, Brian C. Southall, Stephanie Corsi, Smaranda Craciun
Publikováno v:
Tetrahedron Letters. 53:5763-5765
β-Sulfonyl enoates may be synthesized through a one-pot two-step sequence from ethyl propiolate with good to excellent selectivity for the Z isomer. Trialkylamines catalyze thioconjugate additions of aryl thiols, and alkoxides catalyze the addition
Autor:
Smaranda Craciun, Stephanie Corsi, Ana M. Neferu, Brian C. Southall, Ryan J. Sault, C. Wade Downey, Carly J. Mueller, Eric W. Etchill, Christina A. Vivelo
Publikováno v:
ChemInform. 44
β-Sulfonyl enoates may be synthesized through a one-pot two-step sequence from ethyl propiolate with good to excellent selectivity for the Z isomer. Trialkylamines catalyze thioconjugate additions of aryl thiols, and alkoxides catalyze the addition
Autor:
Smaranda Craciun, Carly J. Mueller, Ana M. Neferu, Christina A. Vivelo, C. Wade Downey, Stephanie Corsi
Publikováno v:
ChemInform. 44
In connection with the preceding paper dealing with the preparation of (Z)-β-sulfonyl enoates, the process is extended to the synthesis of bicyclic esters (IV) and (VI) via 1,3-dipolar cycloaddition of cyclopentadiene as a third step.