Indexed keywords
ACYCLIC TERPENOIDS;
DOUBLE BONDS;
ELECTROPHILIC CYCLIZATION;
CARBON;
CYCLIZATION;
SULFONATION;
ORGANIC COMPOUNDS;
1,5 BIS (BENZENESULFONYL) 3,7 DIMETHYL 9 (2,5,5,8A TETRAMETHYL 3,4,4A,5,6,7,8,8A OCTAHYDRONAPHTHALENYL) NONA 2,6 DIENE;
1,5 BIS(BENZENESULFONYL) 3,7,11,15,19 PENTAMETHLICOSA 2,6,10,14,18 PENTAENE;
5 (BENZENESULFONYL) 3,7,11,15,19 PENTAMETHYLICOSA 2,6,10,14,18 PENTAENYL PHENYL SULFIDE;
5,9 BIS (BENZENESULFONYL) 3,7,11,15 TETRAMETHYL HEXADECA 2,6,10,14 TETRAEN 1 OL;
GERANYLGERANIOL;
TERPENOID DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
BROMINATION;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
CYCLIZATION;
SYNTHESIS;
CYCLIZATION;
MASS SPECTROMETRY;
SPECTROPHOTOMETRY, INFRARED;
TERPENES;
2
0003787433
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The Friedel-Craft allylation of the prenyl group proceeded efficiently without cyclization in the coenzyme Q-10 synthesis, due to the presence of a benzenesulfonyl group; see: Min, J.-H, Lee, J.-S, Yang, J.-D, Koo, S. J. Org. Chem. 2003, 68, 7925-7927
The Friedel-Craft allylation of the prenyl group proceeded efficiently without cyclization in the coenzyme Q-10 synthesis, due to the presence of a benzenesulfonyl group; see: Min, J.-H.; Lee, J.-S.; Yang, J.-D.; Koo, S. J. Org. Chem. 2003, 68, 7925-7927.
12
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Minowa, N.5
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For another stereoselective chain-extension method for 12a, see: Jin, Y.; Roberts, F. G.; Coates, R. M. Org. Synth. 2007, 84, 43-57.
For another stereoselective chain-extension method for 12a, see: Jin, Y.; Roberts, F. G.; Coates, R. M. Org. Synth. 2007, 84, 43-57.
27
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The controlled cyclization of compound 13b also worked to give the corresponding monocyclization product in 63% yield, which was 21% lower than that of the cyclization of disulfone 3b, presumably due to instability of the C-S bond under an acidic condition.
The controlled cyclization of compound 13b also worked to give the corresponding monocyclization product in 63% yield, which was 21% lower than that of the cyclization of disulfone 3b, presumably due to instability of the C-S bond under an acidic condition.