244
302. Castro SJ, Garcia ME, Padron JM, Navarro-Vazquez A, Gil RR, Nicotra VE (2018)
Phytochemical study of Senecio volckmannii assisted by CASE-3D with residual dipolar
couplings and isotropic
1 H/
13
C NMR chemical shifts. J Nat Prod 81:2329
303. Illarionova I, Wang L, Yang QE (2017) Ligularia muliensis (Asteraceae, Senecioneae) is
merged with L. tsangchanensis. Phytotaxa 299:169
304. Hillis DM, Dixon MT (1991) Ribosomal DNA: Molecular evolution and phylogenetic inference. Quart Rev Biol 66:411
305. Manen JF, Savolainen V, Simon P (1994) The atpB and rbcL promoters in plastid DNAs of a
wide dicot range. J Mol Evol 38:577
306. Yu JJ, Kuroda C, Gong X (2014) Natural hybridization and introgression between Ligularia
cymbulifera and L. tongolensis (Asteraceae, Senecionae) in four different locations. PloS One
9:e115167
307. Heathcock HC (1973) Total synthesis of sesquiterpenes. In: ApSimon J (ed) The Total
Synthesis of Natural Products, vol 2. John Wiley and Sons, New York, p 361
308. Pinder AR (1977) The chemistry of the eremophilane and related sesquiterpenes. In: Herz W,
Grisebach H, Kirby GW (eds) Progress in the Chemistry of Organic Natural Products, vol 34.
Springer, Vienna, New York, p 81
309. Yamakawa H, Satoh T (1980) The total synthesis of natural products. J Synth Org Chem
Jpn 38:783
310. Yamakawa K, Satoh T (1977) Studies on terpenoids and related alicyclic compounds. X. Total
synthesis of sesquiterpenoids, (±)-ligularone. Chem Pharm Bull 25:2535
311. Yamakawa K, Satoh T (1978) Studies on terpenoids and related alicyclic compounds.
XVI. Total syntheses of furanosesquiterpenes: (±)-furanoeremophilane, (±)-furanoligularenone, (±)-9,10-dehydrofuranoeremophilane, (±)-3β-hydroxyeremophilane, and
(±)-3β-furanoligularenol. Chem Pharm Bull 26:3704
312. Yamakawa K, Satoh T (1979) Studies on terpenoids and related alicyclic compounds.
XVIII. Stereoselective synthesis of (±)-furanofukinol and (±)-petasalbin. Chem Pharm
Bull 27:1747
313. Yamakawa K, Kobayashi M, Hinata S, Satoh T (1980) Studies on the terpenoids and related
alicyclic compounds. XXIII. Total syntheses of (±)-phomenone, (±)-3-epiphomenone,
(±)-ligularenolide, and (±)-furanoligularanone. Chem Pharm Bull 28:3265
314. Yamakawa K, Satoh T (1981) Studies on the terpenoids and related alicyclic
compounds.
XXVI.
Total
synthesis
of
highly
oxygenated
furanoeremophilanes: (±)-6β-hydroxy-1,10-dehydrofuranoeremophylan-9-one, (±)-decompostin, (±)-dihydrodecompostin, (±)-adenostylone, (±)-3β,6β-dipropionyloxyeuryopsin,
(±)-3β,6β-dihydroxy-10βH-furanoeremophilan-9-one, and (±)-3β,6β-dihydroxy-10αHfuranoeremophilan-9-one. Chem Pharm Bull 29:3474
315. Kitagawa I, Yamazoe Y, Takeda R, Yoshioka I (1972) Conversion of dihydroalantolactone to
eremophilane-type derivatives. Biogenetic-type transformation. Tetrahedron Lett:4843
316. Kitagawa I, Shibuya H, Yamazoe Y, Takeno H, Yoshioka I (1974) Conversion of dihydroalantolactone to tetrahydroligularenolide. Biogenetic-type transformation of eudesmanolide to
eremophilanolide. Tetrahedron Lett 15:111
317. Tada M, Sugimoto Y, Takahashi T (1980) Total synthesis of furanoeremophilane and
14- norfuranoeudesmane derivatives by a route involving alkylation of 2,4-dimethyl-3-furoic
acid. Bull Chem Soc Jpn 53:2966
318. Torii S, Inokuchi T, Kawai K (1979) Functionalization of trans-decalin. II. A synthesis of
dl-isopetasol from trans-5-oxodecalin-8α,2-carbolactone. Bull Chem Soc Jpn 52:861
319. Hagiwara H, Uda H, Kodama T (1980) Synthetic study on several eremophilane sesquiterpenes using a common intermediate. J Chem Soc Perkin Trans I: 963
320. Näf F, Decorzant R, Thommen W (1982) A stereocontrolled entry to racemic eremophilane
and valencane sesquiterpenes via an intramolecular Diels-Alder reaction. Helv Chim
Acta 65:2212
M. Tori and C. Kuroda
302. Castro SJ, Garcia ME, Padron JM, Navarro-Vazquez A, Gil RR, Nicotra VE (2018)
Phytochemical study of Senecio volckmannii assisted by CASE-3D with residual dipolar
couplings and isotropic
1 H/
13
C NMR chemical shifts. J Nat Prod 81:2329
303. Illarionova I, Wang L, Yang QE (2017) Ligularia muliensis (Asteraceae, Senecioneae) is
merged with L. tsangchanensis. Phytotaxa 299:169
304. Hillis DM, Dixon MT (1991) Ribosomal DNA: Molecular evolution and phylogenetic inference. Quart Rev Biol 66:411
305. Manen JF, Savolainen V, Simon P (1994) The atpB and rbcL promoters in plastid DNAs of a
wide dicot range. J Mol Evol 38:577
306. Yu JJ, Kuroda C, Gong X (2014) Natural hybridization and introgression between Ligularia
cymbulifera and L. tongolensis (Asteraceae, Senecionae) in four different locations. PloS One
9:e115167
307. Heathcock HC (1973) Total synthesis of sesquiterpenes. In: ApSimon J (ed) The Total
Synthesis of Natural Products, vol 2. John Wiley and Sons, New York, p 361
308. Pinder AR (1977) The chemistry of the eremophilane and related sesquiterpenes. In: Herz W,
Grisebach H, Kirby GW (eds) Progress in the Chemistry of Organic Natural Products, vol 34.
Springer, Vienna, New York, p 81
309. Yamakawa H, Satoh T (1980) The total synthesis of natural products. J Synth Org Chem
Jpn 38:783
310. Yamakawa K, Satoh T (1977) Studies on terpenoids and related alicyclic compounds. X. Total
synthesis of sesquiterpenoids, (±)-ligularone. Chem Pharm Bull 25:2535
311. Yamakawa K, Satoh T (1978) Studies on terpenoids and related alicyclic compounds.
XVI. Total syntheses of furanosesquiterpenes: (±)-furanoeremophilane, (±)-furanoligularenone, (±)-9,10-dehydrofuranoeremophilane, (±)-3β-hydroxyeremophilane, and
(±)-3β-furanoligularenol. Chem Pharm Bull 26:3704
312. Yamakawa K, Satoh T (1979) Studies on terpenoids and related alicyclic compounds.
XVIII. Stereoselective synthesis of (±)-furanofukinol and (±)-petasalbin. Chem Pharm
Bull 27:1747
313. Yamakawa K, Kobayashi M, Hinata S, Satoh T (1980) Studies on the terpenoids and related
alicyclic compounds. XXIII. Total syntheses of (±)-phomenone, (±)-3-epiphomenone,
(±)-ligularenolide, and (±)-furanoligularanone. Chem Pharm Bull 28:3265
314. Yamakawa K, Satoh T (1981) Studies on the terpenoids and related alicyclic
compounds.
XXVI.
Total
synthesis
of
highly
oxygenated
furanoeremophilanes: (±)-6β-hydroxy-1,10-dehydrofuranoeremophylan-9-one, (±)-decompostin, (±)-dihydrodecompostin, (±)-adenostylone, (±)-3β,6β-dipropionyloxyeuryopsin,
(±)-3β,6β-dihydroxy-10βH-furanoeremophilan-9-one, and (±)-3β,6β-dihydroxy-10αHfuranoeremophilan-9-one. Chem Pharm Bull 29:3474
315. Kitagawa I, Yamazoe Y, Takeda R, Yoshioka I (1972) Conversion of dihydroalantolactone to
eremophilane-type derivatives. Biogenetic-type transformation. Tetrahedron Lett:4843
316. Kitagawa I, Shibuya H, Yamazoe Y, Takeno H, Yoshioka I (1974) Conversion of dihydroalantolactone to tetrahydroligularenolide. Biogenetic-type transformation of eudesmanolide to
eremophilanolide. Tetrahedron Lett 15:111
317. Tada M, Sugimoto Y, Takahashi T (1980) Total synthesis of furanoeremophilane and
14- norfuranoeudesmane derivatives by a route involving alkylation of 2,4-dimethyl-3-furoic
acid. Bull Chem Soc Jpn 53:2966
318. Torii S, Inokuchi T, Kawai K (1979) Functionalization of trans-decalin. II. A synthesis of
dl-isopetasol from trans-5-oxodecalin-8α,2-carbolactone. Bull Chem Soc Jpn 52:861
319. Hagiwara H, Uda H, Kodama T (1980) Synthetic study on several eremophilane sesquiterpenes using a common intermediate. J Chem Soc Perkin Trans I: 963
320. Näf F, Decorzant R, Thommen W (1982) A stereocontrolled entry to racemic eremophilane
and valencane sesquiterpenes via an intramolecular Diels-Alder reaction. Helv Chim
Acta 65:2212
M. Tori and C. Kuroda