000 01313 a2200385 4500
005 20250515053116.0
264 0 _c20070319
008 200703s 0 0 eng d
022 _a1523-7060
024 7 _a10.1021/ol0627348
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLindel, Thomas
245 0 0 _aTotal synthesis of flustramine C via dimethylallyl rearrangement.
_h[electronic resource]
260 _bOrganic letters
_cJan 2007
300 _a283-6 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAllyl Compounds
_xchemistry
650 0 4 _aAnimals
650 0 4 _aBryozoa
_xchemistry
650 0 4 _aHeterocyclic Compounds, 3-Ring
_xchemical synthesis
650 0 4 _aIndole Alkaloids
650 0 4 _aIndoles
_xchemistry
650 0 4 _aMagnetic Resonance Spectroscopy
_xmethods
650 0 4 _aModels, Molecular
650 0 4 _aMolecular Structure
650 0 4 _aNiobium
_xchemistry
650 0 4 _aOxidation-Reduction
650 0 4 _aSensitivity and Specificity
650 0 4 _aTryptamines
_xchemistry
700 1 _aBräuchle, Laura
700 1 _aGolz, Gregor
700 1 _aBöhrer, Petra
773 0 _tOrganic letters
_gvol. 9
_gno. 2
_gp. 283-6
856 4 0 _uhttps://doi.org/10.1021/ol0627348
_zAvailable from publisher's website
999 _c16782762
_d16782762