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It has been reported in Ref. [2] that the Mitsunobu esterification requires the ortho-phenol unprotected to get the best yield. On the other hand, the RCM reaction usually worked best with the ortho-phenol protected
-
It has been reported in Ref. [2] that the Mitsunobu esterification requires the ortho-phenol unprotected to get the best yield. On the other hand, the RCM reaction usually worked best with the ortho-phenol protected.
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See Supporting Information for detailed preparation of the aromatic scaffolds 4 and 5.
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-
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78650105776
-
-
the RCM reaction of alkene 18 with the Grubbs II catalyst, a substantial amount of the undesired 6-membered ring product was generated
-
In the RCM reaction of alkene 18 with the Grubbs II catalyst, a substantial amount of the undesired 6-membered ring product was generated.
-
-
-
-
46
-
-
78650131787
-
-
Terminal trisubstituted alkene 7 g was used to suppress the undesired 6-membered ring formation under the existence of the Grubbs II catalyst. 7 g can be prepared from citronellal in short steps
-
Terminal trisubstituted alkene 7 g was used to suppress the undesired 6-membered ring formation under the existence of the Grubbs II catalyst. 7 g can be prepared from citronellal in short steps.
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-
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47
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70350514759
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-
50
-
-
78650136200
-
-
50=17.4 μ M)
-
50=17.4 μ M).
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