New Techniques of Structure Elucidation for Sesquiterpenes
307
48. Fatope MO, Nair RS, Marwah RG, Al-Nadhiri HH (2004) New sesquiterpenes from Pluchea
arabica. J Nat Prod 67:1925
49. Wang HB, Zhang HP, Zhou Y, Zuo JP, Qin GW (2005) Sesquiterpenoids from Saussurea
laniceps. J Nat Prod 68:762
50. Arai T, Toda Y, Kato K, Miyamoto K, Hasegawa T, Yamada K, Shigemori H (2013) Artabolide,
a novel polar auxin transport inhibitor isolated from Artemisia absinthium. Tetrahedron
69:7001
51. Sribuhom T, Sriphana U, Thongsri Y, Yenjai C (2015) Chemical constituents from the stems
of Alyxia schlechteri. Phytochem Lett 11:80
52. Helaly SE, Richter C, Thongbai B, Hyde KD, Stadler M (2016) Lentinulactam, a hirsutane
sesquiterpene with an unprecedented lactam modification. Tetrahedron Lett 57:5911
53. Evans L, Hedger J, O’Donnell G, Skelton BW, White AH, Williamson RT, Gibbons S (2010)
Structure elucidation of some highly unusual tricyclic cis-caryophyllane sesquiterpenes from
Marasmiellus troyanus. Tetrahedron Lett 51:5493
54. Huang XC, Li J, Li ZY, Shi L, Guo YW (2008) Sesquiterpenes from the Hainan sponge
Dysidea septosa. J Nat Prod 71:1399
55. Diep CN, Lyakhova EG, Berdyshev DV, Kalinovsky AI, Tu VA, Cuong NX, Nam NH, Minh
CV, Stonik VA (2015) Structures and absolute stereochemistry of guaiane sesquiterpenoids
from the gorgonian Menella woodin. Tetrahedron Lett 56:7001
56. Molinski TF (2010) Microscale methodology for structure elucidation of natural products.
Curr Opin Biotechnol 21:819
57. Nord C, Menkis A, Broberg A (2015) Cytotoxic illudane sesquiterpenes from the fungus
Granulobasidium vellereum (Ellis and Cragin) Jülich. J Nat Prod 78:2559
58. Tchinda AT, Tsala DE, Nga N, Cieckiewicz E, Kiss R, Connolly JD, Frédérich M (2014)
Two new aromadendrane sesquiterpenes from the stem bark of Alafia multiflora. Nat Prod
Commun 9:1673
59. Grienke U, Brkanac SR, Vujˇ ci´ c V, Urban E, Ivankovi´ c S, Stojkovi´ c R, Rollinger JM, Kralj
J, Brozovic A, Stojkovi´ c MR (2018) Biological activity of flavonoids and rare sesquiterpene
lactones isolated from Centaurea ragusina L. Front Pharmacol 9:972
60. Polavarapu PL (2012) Determination of the structure of chiral natural products using vibrational circular dichroism. In: Berova N, Polavarapu PL, Nakanishi K, Woody RW (eds)
Comprehensive chiroptical spectroscopy. Applications in stereochemical analysis of synthetic
compounds, natural products, and biomolecules, vol 2, chapter 11. Wiley, Hoboken, NJ, USA,
p 387
61. Joseph-Nathan P, Gordillo-Román B (2015) Vibrational circular dichroism absolute configuration determination of natural products. In: Kinghorn AD, Falk H, Kobayashi J (eds) Progress
in the chemistry of organic natural products, vol 100. Springer International Publishing, Cham,
Switzerland, p 311
62. Batista JM Jr (2013) Determination of absolute configuration using chiroptical methods. In:
Andrushko V, Andrushko N (eds) Stereoselective synthesis of drugs and natural products, vol
2, chapter 53. Wiley, Hoboken, NJ, USA, p 1571
63. Batista Jr JM, da Silva Bolzani V (2014) Determination of the absolute configuration of natural
product molecules using vibrational circular dichroism. In: Atta-ur-Rahman (ed) Studies in
natural products chemistry, vol 41. Elsevier, Amsterdam, The Netherlands, p 311
64. Batista JM Jr, Blanch EW, da Silva BV (2015) Recent advances in the use of vibrational
chiroptical spectroscopic methods for stereochemical characterization of natural products.
Nat Prod Rep 32:1280
65. Kong LY, Wang P (2013) Determination of the absolute configuration of natural products.
Chin J Nat Med 11:193
66. Santoro E, Mazzeo G, Petrovic AG, Cimmino A, Koshoubu J, Evidente A, Berova N, Superchi
S (2015) Absolute configurations of phytotoxins seiricardine A and inuloxin A obtained by
chiroptical studies. Phytochemistry 116:359
67. Junior FM, Covington CL, de Albuquerque ACF, Lobo JF, Borges RM, de Amorim MB,
Polavarapu PL (2015) Absolute configuration of (–)-centratherin, a sesquiterpenoid lactone,
defined by means of chiroptical spectroscopy. J Nat Prod 78:2617
307
48. Fatope MO, Nair RS, Marwah RG, Al-Nadhiri HH (2004) New sesquiterpenes from Pluchea
arabica. J Nat Prod 67:1925
49. Wang HB, Zhang HP, Zhou Y, Zuo JP, Qin GW (2005) Sesquiterpenoids from Saussurea
laniceps. J Nat Prod 68:762
50. Arai T, Toda Y, Kato K, Miyamoto K, Hasegawa T, Yamada K, Shigemori H (2013) Artabolide,
a novel polar auxin transport inhibitor isolated from Artemisia absinthium. Tetrahedron
69:7001
51. Sribuhom T, Sriphana U, Thongsri Y, Yenjai C (2015) Chemical constituents from the stems
of Alyxia schlechteri. Phytochem Lett 11:80
52. Helaly SE, Richter C, Thongbai B, Hyde KD, Stadler M (2016) Lentinulactam, a hirsutane
sesquiterpene with an unprecedented lactam modification. Tetrahedron Lett 57:5911
53. Evans L, Hedger J, O’Donnell G, Skelton BW, White AH, Williamson RT, Gibbons S (2010)
Structure elucidation of some highly unusual tricyclic cis-caryophyllane sesquiterpenes from
Marasmiellus troyanus. Tetrahedron Lett 51:5493
54. Huang XC, Li J, Li ZY, Shi L, Guo YW (2008) Sesquiterpenes from the Hainan sponge
Dysidea septosa. J Nat Prod 71:1399
55. Diep CN, Lyakhova EG, Berdyshev DV, Kalinovsky AI, Tu VA, Cuong NX, Nam NH, Minh
CV, Stonik VA (2015) Structures and absolute stereochemistry of guaiane sesquiterpenoids
from the gorgonian Menella woodin. Tetrahedron Lett 56:7001
56. Molinski TF (2010) Microscale methodology for structure elucidation of natural products.
Curr Opin Biotechnol 21:819
57. Nord C, Menkis A, Broberg A (2015) Cytotoxic illudane sesquiterpenes from the fungus
Granulobasidium vellereum (Ellis and Cragin) Jülich. J Nat Prod 78:2559
58. Tchinda AT, Tsala DE, Nga N, Cieckiewicz E, Kiss R, Connolly JD, Frédérich M (2014)
Two new aromadendrane sesquiterpenes from the stem bark of Alafia multiflora. Nat Prod
Commun 9:1673
59. Grienke U, Brkanac SR, Vujˇ ci´ c V, Urban E, Ivankovi´ c S, Stojkovi´ c R, Rollinger JM, Kralj
J, Brozovic A, Stojkovi´ c MR (2018) Biological activity of flavonoids and rare sesquiterpene
lactones isolated from Centaurea ragusina L. Front Pharmacol 9:972
60. Polavarapu PL (2012) Determination of the structure of chiral natural products using vibrational circular dichroism. In: Berova N, Polavarapu PL, Nakanishi K, Woody RW (eds)
Comprehensive chiroptical spectroscopy. Applications in stereochemical analysis of synthetic
compounds, natural products, and biomolecules, vol 2, chapter 11. Wiley, Hoboken, NJ, USA,
p 387
61. Joseph-Nathan P, Gordillo-Román B (2015) Vibrational circular dichroism absolute configuration determination of natural products. In: Kinghorn AD, Falk H, Kobayashi J (eds) Progress
in the chemistry of organic natural products, vol 100. Springer International Publishing, Cham,
Switzerland, p 311
62. Batista JM Jr (2013) Determination of absolute configuration using chiroptical methods. In:
Andrushko V, Andrushko N (eds) Stereoselective synthesis of drugs and natural products, vol
2, chapter 53. Wiley, Hoboken, NJ, USA, p 1571
63. Batista Jr JM, da Silva Bolzani V (2014) Determination of the absolute configuration of natural
product molecules using vibrational circular dichroism. In: Atta-ur-Rahman (ed) Studies in
natural products chemistry, vol 41. Elsevier, Amsterdam, The Netherlands, p 311
64. Batista JM Jr, Blanch EW, da Silva BV (2015) Recent advances in the use of vibrational
chiroptical spectroscopic methods for stereochemical characterization of natural products.
Nat Prod Rep 32:1280
65. Kong LY, Wang P (2013) Determination of the absolute configuration of natural products.
Chin J Nat Med 11:193
66. Santoro E, Mazzeo G, Petrovic AG, Cimmino A, Koshoubu J, Evidente A, Berova N, Superchi
S (2015) Absolute configurations of phytotoxins seiricardine A and inuloxin A obtained by
chiroptical studies. Phytochemistry 116:359
67. Junior FM, Covington CL, de Albuquerque ACF, Lobo JF, Borges RM, de Amorim MB,
Polavarapu PL (2015) Absolute configuration of (–)-centratherin, a sesquiterpenoid lactone,
defined by means of chiroptical spectroscopy. J Nat Prod 78:2617