Synthesis, Table of Contents Synthesis 2009(3): 512-512 DOI: 10.1055/s-0028-1083326 ADDENDA © Georg Thieme Verlag Stuttgart ˙ New York Synthesis and Olfactory Evaluation of (4aR*,8aR*)-1,1,8a-Trimethyl-decahydronaphthalen-4a-ol: A cis-Decalol Intersection Structure of (-)-Patchoulol and (5R*,6S*)-1,1,6-Trimethylspiro[4.5]decan-6-ol Recommend Article Abstract Full Text PDF Download All articles of this category Correction to: Synthesis and Olfactory Evaluation of (4aR*,8aR*)-1,1,8a-Trimethyldecahydronaphthalen-4a-ol: A cis-Decalol Intersection Structure of (-)-Patchoulol and (5R*,6S*)-1,1,6-Trimethylspiro[4.5]decan-6-olSynthesis 2009; 2009(01): 62-68DOI: 10.1055/s-0028-1083269 Jahnke Astrid. Burschka Christian. Tacke Reinhold. Kraft Philip. Synthesis 2009, 62 Inadvertently, instead of (-)-patchoulol, the (+)-enantiomer was drawn in Figures [¹] and [²] . As the target compound and all intermediates are racemates, this has no influence on the results, still Figures [¹] and [²] should be replaced by the correct representations below. For the sake of better correlation, the opposite enantiomer has also been delineated for racemic compounds. The authors apologize for this mistake. Figure 1 Patchouli odorants, decalin odorants, and the derivation of the cis-decalol intersection target structure 4 Figure 2 Biflexible superposition analysis of (-)-patchoulol (1, depicted in silver) on the patchouli-smelling (5R*,6S*)-1,1,6-trimethylspiro[4.5]decan-6-ol (3, displayed in gold) with the MOE 2007.09 software package Figures All articles of this category Figure 1 Patchouli odorants, decalin odorants, and the derivation of the cis-decalol intersection target structure 4 Figure 2 Biflexible superposition analysis of (-)-patchoulol (1, depicted in silver) on the patchouli-smelling (5R*,6S*)-1,1,6-trimethylspiro[4.5]decan-6-ol (3, displayed in gold) with the MOE 2007.09 software package
