A total synthesis of 1,14-herbertenediol via 11-epi-herbertenolide, and a formal total synthesis of tochuinyl acetate and dihydrotochuinyl acetate, employing a ring-closing metathesis reaction based methodology, are described
Details of the first total synthesis of the marine natural product dihydrotochuinyl acetate is descr...
A combination of Ireland ester Claisen rearrangement and ring-closing metathesis (RCM) reactions has...
A combination of Ireland ester Claisen rearrangement and ring-closing metathesis (RCM) reactions has...
A total synthesis of 1,14-herbertenediol via 11-epi-herbertenolide, and a formal total synthesis of ...
A total synthesis of 1,14-herbertenediol via 11-epi-herbertenolide, and a formal total synthesis of ...
A formal total synthesis of (±)-1,13-herbertenediol, employing a ring-closing metathesis reaction of...
A formal total synthesis of $(\pm)$-1,13-herbertenediol, employing a ring-closing metathesis reactio...
A formal total synthesis of $(\pm)$-1,13-herbertenediol, employing a ring-closing metathesis reactio...
A formal synthesis of the aromatic sesquiterpenes (+/-)-herbertene and (+/-)-cuparenesis accomplishe...
A formal synthesis of the aromatic sesquiterpenes (+/-)-herbertene and (+/-)-cuparenesis accomplishe...
Total synthesis of α-herbertenol, β-herbertenol and 1,13-herbertenediol, employing a Claisen rearran...
An efficient methodology for the synthesis of the aromatic sesquiterpenes (+/-)-herbertene, (+/-)-al...
An efficient methodology for the synthesis of the aromatic sesquiterpenes (+/-)-herbertene, (+/-)-al...
An efficient methodology for the synthesis of the aromatic sesquiterpenes (±)-herbertene, (±)-α-herb...
A combination of Ireland ester Claisen rearrangement and ring-closing metathesis (RCM) reactions has...
Details of the first total synthesis of the marine natural product dihydrotochuinyl acetate is descr...
A combination of Ireland ester Claisen rearrangement and ring-closing metathesis (RCM) reactions has...
A combination of Ireland ester Claisen rearrangement and ring-closing metathesis (RCM) reactions has...
A total synthesis of 1,14-herbertenediol via 11-epi-herbertenolide, and a formal total synthesis of ...
A total synthesis of 1,14-herbertenediol via 11-epi-herbertenolide, and a formal total synthesis of ...
A formal total synthesis of (±)-1,13-herbertenediol, employing a ring-closing metathesis reaction of...
A formal total synthesis of $(\pm)$-1,13-herbertenediol, employing a ring-closing metathesis reactio...
A formal total synthesis of $(\pm)$-1,13-herbertenediol, employing a ring-closing metathesis reactio...
A formal synthesis of the aromatic sesquiterpenes (+/-)-herbertene and (+/-)-cuparenesis accomplishe...
A formal synthesis of the aromatic sesquiterpenes (+/-)-herbertene and (+/-)-cuparenesis accomplishe...
Total synthesis of α-herbertenol, β-herbertenol and 1,13-herbertenediol, employing a Claisen rearran...
An efficient methodology for the synthesis of the aromatic sesquiterpenes (+/-)-herbertene, (+/-)-al...
An efficient methodology for the synthesis of the aromatic sesquiterpenes (+/-)-herbertene, (+/-)-al...
An efficient methodology for the synthesis of the aromatic sesquiterpenes (±)-herbertene, (±)-α-herb...
A combination of Ireland ester Claisen rearrangement and ring-closing metathesis (RCM) reactions has...
Details of the first total synthesis of the marine natural product dihydrotochuinyl acetate is descr...
A combination of Ireland ester Claisen rearrangement and ring-closing metathesis (RCM) reactions has...
A combination of Ireland ester Claisen rearrangement and ring-closing metathesis (RCM) reactions has...
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