Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Francesca E. Blum"'
Publikováno v:
ChemInform. 47
A novel, high-yielding, one-step synthesis of 2-chloroquinazolin-4-ols and analogous bicycles from 2-aminoamides using thiophosgene is described. The scope of the reaction includes aminothioamides, amino acids, and fused heterocycle derivatives, furn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f31f71dd8a0da4f7bdae2b840b5b464
https://doi.org/10.1002/chin.201608185
https://doi.org/10.1002/chin.201608185
Publikováno v:
Tetrahedron. 64:4711-4717
A convenient synthesis of the phytotoxic natural product epipyriculol has been accomplished in 17 steps from methyl l -tartrate. The synthetic strategy is based upon the use of a butanediacetal-protected scaffold as central core from which the alkeny
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed0797454fd358382f34e1f68fe23473
https://doi.org/10.1016/j.tet.2008.01.115
https://doi.org/10.1016/j.tet.2008.01.115
Publikováno v:
Tetrahedron. 64:2348-2358
A new method for the synthesis of dienes and enynes containing chiral 1,2-diols is described. The strategy is based on the Pd-catalysed cross-coupling reactions of a series of vinyl and alkynyl asymmetric butanediacetal-protected building blocks. Aft
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74b09bec931bb0ecfd37d6c9ab4b1384
https://doi.org/10.1016/j.tet.2008.01.010
https://doi.org/10.1016/j.tet.2008.01.010
Publikováno v:
Organic letters. 17(19)
A novel, high-yielding, one-step synthesis of 2-chloroquinazolin-4-ols and analogous bicycles from 2-aminoamides using thiophosgene is described. The scope of the reaction includes aminothioamides, amino acids, and fused heterocycle derivatives, furn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35ac35330469e26bc2b05dc41c9ac7e4
https://pubmed.ncbi.nlm.nih.gov/26360817
https://pubmed.ncbi.nlm.nih.gov/26360817
Publikováno v:
ChemInform. 39
A convenient synthesis of the phytotoxic natural product epipyriculol has been accomplished in 17 steps from methyl l -tartrate. The synthetic strategy is based upon the use of a butanediacetal-protected scaffold as central core from which the alkeny
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67258ca4e3a7c542958bd532dcc4f838
https://doi.org/10.1002/chin.200840207
https://doi.org/10.1002/chin.200840207