000 01273 a2200301 4500
005 20250517025208.0
264 0 _c20160126
008 201601s 0 0 eng d
022 _a1521-3773
024 7 _a10.1002/anie.201501608
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRummelt, Stephan M
245 0 0 _aSelective Formation of a Trisubstituted Alkene Motif by trans-Hydrostannation/Stille Coupling: Application to the Total Synthesis and Late-Stage Modification of 5,6-Dihydrocineromycin B.
_h[electronic resource]
260 _bAngewandte Chemie (International ed. in English)
_cMay 2015
300 _a6241-5 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAlkenes
_xchemical synthesis
650 0 4 _aBiological Products
_xchemical synthesis
650 0 4 _aChemistry Techniques, Synthetic
650 0 4 _aLactones
_xchemical synthesis
650 0 4 _aModels, Molecular
650 0 4 _aStreptomyces
_xchemistry
700 1 _aPreindl, Johannes
700 1 _aSommer, Heiko
700 1 _aFĂĽrstner, Alois
773 0 _tAngewandte Chemie (International ed. in English)
_gvol. 54
_gno. 21
_gp. 6241-5
856 4 0 _uhttps://doi.org/10.1002/anie.201501608
_zAvailable from publisher's website
999 _c24797966
_d24797966