Literature DB >> 11456557

Aplydactone, a new sesquiterpenoid with an unprecedented carbon skeleton from the sea hare Aplysia dactylomela, and its cargill-like rearrangement.

S N Fedorov1, O S Radchenko, L K Shubina, A I Kalinovsky, A V Gerasimenko, D Y Popov, V A Stonik.   

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Year:  2001        PMID： 11456557     DOI： 10.1021/ja003254t

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN： 0002-7863            Impact factor:   15.419


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  5 in total

Review 1.  Catalytic Enantioselective Dihalogenation in Total Synthesis.

Authors:  Matthew L Landry; Noah Z Burns
Journal:  Acc Chem Res       Date:  2018-04-17       Impact factor: 22.384

2.  A general enantioselective route to the chamigrene natural product family.

Authors:  David E White; Ian C Stewart; Brinton A Seashore-Ludlow; Robert H Grubbs; Brian M Stoltz
Journal:  Tetrahedron       Date:  2010-03-26       Impact factor: 2.457

3.  A Unified Approach for the Enantioselective Synthesis of the Brominated Chamigrene Sesquiterpenes.

Authors:  Alexander J Burckle; Vasil H Vasilev; Noah Z Burns
Journal:  Angew Chem Int Ed Engl       Date:  2016-08-10       Impact factor: 15.336

4.  Unravelling Photochemical Relationships Among Natural Products from Aplysia dactylomela.

Authors:  Bryan S Matsuura; Patrick Kölle; Dirk Trauner; Regina de Vivie-Riedle; Robin Meier
Journal:  ACS Cent Sci       Date:  2016-12-19       Impact factor: 14.553

Review 5.  Total syntheses of strained polycyclic terpenes.

Authors:  Gleb A Chesnokov; Karl Gademann
Journal:  Chem Commun (Camb)       Date:  2022-04-19       Impact factor: 6.065
  5 in total

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