Journal of the Chemical Society. Chemical communications p. 734 - 735 (1981)
Update date:2022-08-03
Topics: Yield NMR spectroscopy Enantiomeric excess (ee) Stereoselective synthesis Total synthesis Optical rotation Asymmetric catalysis HPLC (high-performance liquid chromatography) Protecting group X-ray crystallography Retrosynthetic analysis Chiral Auxiliary Ring-Closing Metathesis Diterpene Lactonization Stereocenter Marine Natural Product
Imamura, Paulo M.
Sierra, Manuel Gonzalez
Ruveda, Edmundo A.
The synthesis of (+)-isoagatholactone (1) from (+)-manool (4) via the key intermediate ent-methyl isocopalate (2) is described.
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Doi:10.1007/BF00988238
(1979)Doi:10.1021/jo00330a048
(1981)Doi:10.1016/j.bmc.2003.10.004
(2004)Doi:10.1039/DT9780000110
()Doi:10.1016/0032-3950(78)90361-1
(1978)Doi:10.1021/ja01138a006
(1952)
