Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sofia S. Salim"'
Autor:
Richard C. D. Brown, Vachiraporn Ajavakom, Potchanee Pandokrak, Sofia S. Salim, Gamal A. I. Moustafa, Richard K. Bellingham, Joseph T. Hill-Cousins, Anawat Ajavakom
Publikováno v:
Synlett. 33:1453-1457
A Grubbs II catalyst mediated ring-closing metathesis (RCM) of monobrominated dienes is reported to proceed in moderate to good yields (40–80%) where the linking chain contains five atoms, leading to carbocyclic and heterocyclic seven-membered brom
Autor:
Sofia S. Salim, Richard C. D. Brown, Youssef M. Bakar, Joseph T. Hill-Cousins, Mark E. Light, Richard K. Bellingham
Publikováno v:
Tetrahedron. 70:3700-3706
Ring-closing metathesis (RCM) and sequential Yb(OTf)3 promoted Diels–Alder reactions of sulfamide-linked enynes proceeded selectively in one-pot to afford a series of bicyclic and tricyclic sulfamides. Excellent levels of diastereoselectivity are o
Publikováno v:
Organic Letters. 5:3403-3406
[reaction: see text] Ring-closing metathesis (RCM) of vinyl fluoride-containing dienes in the presence of ruthenium alkylidene carbene complex 11 proceeded efficiently to give six- and seven-membered cyclic vinyl fluorides. The RCM reaction was used
Autor:
Richard C. D. Brown, Mark E. Light, Youssef M. Bakar, Joseph T. Hill-Cousins, Richard K. Bellingham, Sofia S. Salim
Publikováno v:
ChemInform. 45
A one-pot procedure for the formation of polycyclic sulfamides via an enyne ring-closing metathesis—Diels—Alder sequence is developed, giving rise to the endo-adducts as the sole observed diastereoisomers.
Publikováno v:
ChemInform. 35
Ring-closing metathesis (RCM) of sulfamide-linked enynes 7, 11 and 12 containing disubstituted alkynes afforded a series of novel 7-membered cyclic sulfamides 13-15 in good yield. Substrates 5, 9 and 10 containing mono-substituted dlkynes gave either
Autor:
Salim S; Practice Education Facilitator, North Somerset Community Partnership.
Publikováno v:
British journal of community nursing [Br J Community Nurs] 2014 Sep; Vol. 19 (9), pp. 453-557.