308
J. C. Pardo-Novoa and C. M. Cerda-García-Rojas
68. Ortega AR, Sánchez-Castellanos M, Pérez-Hernández N, Robles-Zepeda RE, Joseph-Nathan
P, Quijano L (2016) Relative stereochemistry and absolute configuration of farinosin, a
eudesmanolide from Encelia farinosa. Chirality 28:415
69. Matsuo Y, Maeda S, Ohba C, Fukaya H, Mimaki Y (2016) Vetiverianines A, B, and C:
sesquiterpenoids from Vetiveria zizanioides roots. J Nat Prod 79:2175
70. Polavarapu PL, Covington CL, Raghavan V (2017) To avoid chasing incorrect chemical
structures of chiral compounds: Raman optical activity and vibrational circular dichroism
spectroscopies. ChemPhysChem 18:2459
71. San Feliciano A, Medarde M, Miguel del Corral JM, Aramburu A, Gordaliza M, Barrero AF
(1989) Aquatolide. A new type of humulane-related sesquiterpene lactone. Tetrahedron Lett
30:2851
72. Lodewyk MW, Soldi C, Jones PB, Olmstead MM, Rita J, Shaw JT, Tantillo DJ (2012) The
correct structure of aquatolide–experimental validation of a theoretically predicted structural
revision. J Am Chem Soc 134:18550
73. Pauli GF, Niemitz M, Bisson J, Lodewyk MW, Soldi C, Shaw JT, Tantillo DJ, Saya JM,
Vos K, Kleinnijenhuis RA, Hiemstra H, Chen SN, McAlpine JB, Lankin DC, Friesen JB
(2016) Toward structural correctness: aquatolide and the importance of 1D proton NMR FID
archiving. J Org Chem 81:878
74. Medina RP, Araujo AR, Batista JM, Cardoso CL, Seidl C, Vilela AFL, Domingos HV,
Costa-Lotufo LV, Andersen RJ, Silva DHS (2019) Botryane terpenoids produced by
Nemania bipapillata, an endophytic fungus isolated from red alga Asparagopsis taxiformis -
Falkenbergia stage. Sci Rep 9:12318
75. Lydon CA, Mathivathanan L, Sanchez J, dos Santos LAH, Sauvage T, Gunasekera SP, Paul
VJ, Berry JP (2020) Eudesmacarbonate, a eudesmane-type sesquiterpene from a marine
filamentous cyanobacterial mat (oscillatoriales) in the Florida Keys. J Nat Prod 83:2030
76. Li XC, Ferreira D, Ding Y (2010) Determination of absolute configuration of natural products:
theoretical calculation of electronic circular dichroism as a tool. Curr Org Chem 14:1678
77. Xi FM, Ma SG, Liu YB, Li L, Yu SS (2016) Artaboterpenoids A and B, bisabolene-derived
sesquiterpenoids from Artabotrys hexapetalus. Org Lett 18:3374
78. Yu Y, Gao H, Dai Y, Xiao GK, Zhu HJ, Yao XS (2011) Guaiane-type sesquiterpenoid
glucosides from Gardenia jasminoides Ellis. Magn Reson Chem 49:258
79. Ma SG, Li M, Lin MB, Li L, Liu YB, Qu J, Li Y, Wang XJ, Wang RB, Xu S, Hou Q, Yu SS
(2017) Illisimonin A, a caged sesquiterpenoid with a tricyclo[5.2.1.0 1,6 decane skeleton from
the fruits of Illicium simonsii. Org Lett 19:6160
80. Du Y, Pearce KC, Dai Y, Krai P, Dalal S, Cassera MB, Goetz M, Crawford TD, Kingston
DGI (2017) Antiplasmodial sesquiterpenoid lactones from Trichospira verticillata: structure
elucidation by spectroscopic methods and comparison of experimental and calculated ECD
data. J Nat Prod 80:1639
81. Ren Y, Munoz Acuña U, Jiménez F, García R, Mejía M, Chai H, Gallucci JC, Farnsworth NR,
Soejarto DD, Carcache de Blanco EJ, Kinghorn AD (2012) Cytotoxic and NF-κB inhibitory
sesquiterpene lactones from Piptocoma rufescens. Tetrahedron 68:2671
82. Inose K, Tanaka K, Yamada T, Koshino H, Hashimoto M (2019) Isolation of peribysins O, P,
and Q from Periconia macrospinosa KT3863 and configurational reinvestigation of peribysin
E diacetate from Periconia byssoides OUPS-N133. J Nat Prod 82:911
83. Reinhardt JK, Klemd AM, Danton O, De Mieri M, Smieško M, Huber R, Bürgi T, Gründemann
C, Hamburger M (2019) Sesquiterpene lactones from Artemisia argyi: absolute configuration
and immunosuppressant activity. J Nat Prod 82:1424
84. Zhou CX, Zhang LS, Chen FF, Wu HS, Mo JX, Gan LS (2017) Terpenoids from Curcuma
wenyujin increased glucose consumption on HepG2 cells. Fitoterapia 121:141
85. Hassan Z, Hussain H, Ahmad VU, Anjum S, Pescitelli G, Kurtán T, Krohn K (2007) Absolute
configuration of 1β,10β-epoxydesacetoxymatricarin isolated from Carthamus oxycantha by
means of TDDFT CD calculations. Tetrahedron: Asymmetry 18:2905
J. C. Pardo-Novoa and C. M. Cerda-García-Rojas
68. Ortega AR, Sánchez-Castellanos M, Pérez-Hernández N, Robles-Zepeda RE, Joseph-Nathan
P, Quijano L (2016) Relative stereochemistry and absolute configuration of farinosin, a
eudesmanolide from Encelia farinosa. Chirality 28:415
69. Matsuo Y, Maeda S, Ohba C, Fukaya H, Mimaki Y (2016) Vetiverianines A, B, and C:
sesquiterpenoids from Vetiveria zizanioides roots. J Nat Prod 79:2175
70. Polavarapu PL, Covington CL, Raghavan V (2017) To avoid chasing incorrect chemical
structures of chiral compounds: Raman optical activity and vibrational circular dichroism
spectroscopies. ChemPhysChem 18:2459
71. San Feliciano A, Medarde M, Miguel del Corral JM, Aramburu A, Gordaliza M, Barrero AF
(1989) Aquatolide. A new type of humulane-related sesquiterpene lactone. Tetrahedron Lett
30:2851
72. Lodewyk MW, Soldi C, Jones PB, Olmstead MM, Rita J, Shaw JT, Tantillo DJ (2012) The
correct structure of aquatolide–experimental validation of a theoretically predicted structural
revision. J Am Chem Soc 134:18550
73. Pauli GF, Niemitz M, Bisson J, Lodewyk MW, Soldi C, Shaw JT, Tantillo DJ, Saya JM,
Vos K, Kleinnijenhuis RA, Hiemstra H, Chen SN, McAlpine JB, Lankin DC, Friesen JB
(2016) Toward structural correctness: aquatolide and the importance of 1D proton NMR FID
archiving. J Org Chem 81:878
74. Medina RP, Araujo AR, Batista JM, Cardoso CL, Seidl C, Vilela AFL, Domingos HV,
Costa-Lotufo LV, Andersen RJ, Silva DHS (2019) Botryane terpenoids produced by
Nemania bipapillata, an endophytic fungus isolated from red alga Asparagopsis taxiformis -
Falkenbergia stage. Sci Rep 9:12318
75. Lydon CA, Mathivathanan L, Sanchez J, dos Santos LAH, Sauvage T, Gunasekera SP, Paul
VJ, Berry JP (2020) Eudesmacarbonate, a eudesmane-type sesquiterpene from a marine
filamentous cyanobacterial mat (oscillatoriales) in the Florida Keys. J Nat Prod 83:2030
76. Li XC, Ferreira D, Ding Y (2010) Determination of absolute configuration of natural products:
theoretical calculation of electronic circular dichroism as a tool. Curr Org Chem 14:1678
77. Xi FM, Ma SG, Liu YB, Li L, Yu SS (2016) Artaboterpenoids A and B, bisabolene-derived
sesquiterpenoids from Artabotrys hexapetalus. Org Lett 18:3374
78. Yu Y, Gao H, Dai Y, Xiao GK, Zhu HJ, Yao XS (2011) Guaiane-type sesquiterpenoid
glucosides from Gardenia jasminoides Ellis. Magn Reson Chem 49:258
79. Ma SG, Li M, Lin MB, Li L, Liu YB, Qu J, Li Y, Wang XJ, Wang RB, Xu S, Hou Q, Yu SS
(2017) Illisimonin A, a caged sesquiterpenoid with a tricyclo[5.2.1.0 1,6 decane skeleton from
the fruits of Illicium simonsii. Org Lett 19:6160
80. Du Y, Pearce KC, Dai Y, Krai P, Dalal S, Cassera MB, Goetz M, Crawford TD, Kingston
DGI (2017) Antiplasmodial sesquiterpenoid lactones from Trichospira verticillata: structure
elucidation by spectroscopic methods and comparison of experimental and calculated ECD
data. J Nat Prod 80:1639
81. Ren Y, Munoz Acuña U, Jiménez F, García R, Mejía M, Chai H, Gallucci JC, Farnsworth NR,
Soejarto DD, Carcache de Blanco EJ, Kinghorn AD (2012) Cytotoxic and NF-κB inhibitory
sesquiterpene lactones from Piptocoma rufescens. Tetrahedron 68:2671
82. Inose K, Tanaka K, Yamada T, Koshino H, Hashimoto M (2019) Isolation of peribysins O, P,
and Q from Periconia macrospinosa KT3863 and configurational reinvestigation of peribysin
E diacetate from Periconia byssoides OUPS-N133. J Nat Prod 82:911
83. Reinhardt JK, Klemd AM, Danton O, De Mieri M, Smieško M, Huber R, Bürgi T, Gründemann
C, Hamburger M (2019) Sesquiterpene lactones from Artemisia argyi: absolute configuration
and immunosuppressant activity. J Nat Prod 82:1424
84. Zhou CX, Zhang LS, Chen FF, Wu HS, Mo JX, Gan LS (2017) Terpenoids from Curcuma
wenyujin increased glucose consumption on HepG2 cells. Fitoterapia 121:141
85. Hassan Z, Hussain H, Ahmad VU, Anjum S, Pescitelli G, Kurtán T, Krohn K (2007) Absolute
configuration of 1β,10β-epoxydesacetoxymatricarin isolated from Carthamus oxycantha by
means of TDDFT CD calculations. Tetrahedron: Asymmetry 18:2905