The Role of Total Synthesis in Structure …
53
71. Maltese F, van der Krooy F, Verpoorte R (2009) Solvent derived artifacts in natural products
chemistry. Nat Prod Commun 4:447
72. Harada N (2017) Chiral molecular science: how were the absolute configurations of chiral
molecules determined? “Experimental results and theories”. Chirality 29:774
73. Parker D (1991) NMR determination of enantiomeric purity. Chem Rev 91:1441
74. Dale JA, Mosher HS (1973) Nuclear magnetic resonance enantiomer regents. Configurational
correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate,
O-methylmandelate, and α-methoxy-α-trifluoromethylphenylacetate (MTPA) esters. J Am
Chem Soc 95:512
75. Theil F, Costisella B, Schick H (1992) A correlation of configuration and 19 F-NMR chemical
shifts of (R)-(+)-Mosher esters of chiral cyclopentanediol derivatives. J Prakt Chem 334:85
76. Bhilabutra W, Techowisan T, Peberdy JF, Lumyong S (2007) Antimicrobial activity of
bioactive compounds from Periconia siamensis CMUGE015. Res J Microbiol 2:749
77. Fun H-K, Bhilabutra W, Tuntiwachwuttikul P, Chantrapromma S (2006) 5,8-Dihydroxy-10methyl-5,8,9,10-tetrahydro-2H-oxecin-2-one. Acta Cryst E 62:o2478
78. Evidente A, Cimmino A, Berestetskiy A, Andolfi A, Motta A (2008) Stagonolides G−I and
modiolide A, nonenolides produced by Stagonospora cirsii, a potential mycoherbicide for
Cirsium arvense. J Nat Prod 71:1897
79. Greve H, Schupp PJ, Eguereva E, Kehraus S, König GM (2008) Ten-membered lactones from
the marine-derived fungus Curvularia sp. J Nat Prod 71:1651
80. Mondol MAM, Farthouse J, Islam MT, Schüffler A, Laatsch H (2017) Metabolites from the
endophytic fungus Curvularia sp. M12 act as motility inhibitors against Phytophthora capsici
zoospores. J Nat Prod 80:347
81. Zheng C-J, Shao C-L, Chen M, Niu Z-G, Zhao D-L, Wang C-Y (2015) Merosesquiterpenoids and ten-membered macrolides from a soft coral-derived Lophiostoma sp. fungus.
Chem Biodivers 12:1407
82. Quang TH, Kim DC, Van Kiem P, Van Minh C, Nhiem NX, Tai BH, Yen PH, Thi Thanh
Ngan N, Kim HJ, Oh H (2018) Macrolide and phenolic metabolites from the marine-derived
fungus Paraconiothyrium sp. VK-13 with anti-inflammatory activity. J Antibiot 71:826
83. Pescitelli G (2018) For a correct application of the CD exciton chirality method: the case of
laucysteinamide A. Mar Drugs 16:388
84. Matsuda M, Yamazaki T, Fuhshuku K-I, Sugai T (2007) First total synthesis of modiolide
A, based on the whole-cell yeast-catalyzed asymmetric reduction of a propargyl ketone.
Tetrahedron 63:8752
85. Gil A, Albericio F, Álvarez M (2017) Role of the Nozaki–Hiyama–Takai–Kishi reaction in
the synthesis of natural products. Chem Rev 117:8420
86. Mohapatra DK, Dash U, Naidu PR, Yadav JS (2009) Stereoselective total synthesis of
stagonolide C and formal total synthesis of modiolide A. Synlett 2129
87. Yuzikhin O, Mitina G, Berestetskiy A (2007) Herbicidal potential of stagonolide, a new
phytotoxic nonenolide from Stagonospora cirsii. J Agric Food Chem 55:7707
88. Berestetskiy A, Dmitriev A, Mitina G, Lisker I, Andolfi A, Evidente A (2008) Nonenolides
and cytochalasins with phytotoxic activity against Cirsium arvense and Sonchus arvensis: a
structure–activity relationships study. Phytochemistry 69:953
89. Evidente A, Cimmino A, Berestetskiy A, Mitina G, Andolfi A, Motta A (2008) Stagonolides
B–F, nonenolides produced by Stagonospora cirsii, a potential mycoherbicide of Cirsium
arvense. J Nat Prod 71:31
90. Dalinova A, Dubovik V, Chisty L, Kochura D, Ivanov A, Smirnov S, Petrova M, Zolotarev
A, Evidente A, Berestetskiy A (2019) Stagonolides J and K and stagochromene A, two new
natural substituted nonenolides and a new disubstituted chromene-4,5-dione isolated from
Stagonospora cirsii S-47 proposed for the biocontrol of Sonchus arvensis. J Agric Food
Chem 67:13040
91. Rivero-Cruz JF, García-Aguirre G, Cerda-García-Rojas CM, Mata R (2000) Conformational
behavior and absolute stereostructure of two phytotoxic nonenolides from the fungus Phoma
herbarum. Tetrahedron 56:5337
53
71. Maltese F, van der Krooy F, Verpoorte R (2009) Solvent derived artifacts in natural products
chemistry. Nat Prod Commun 4:447
72. Harada N (2017) Chiral molecular science: how were the absolute configurations of chiral
molecules determined? “Experimental results and theories”. Chirality 29:774
73. Parker D (1991) NMR determination of enantiomeric purity. Chem Rev 91:1441
74. Dale JA, Mosher HS (1973) Nuclear magnetic resonance enantiomer regents. Configurational
correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate,
O-methylmandelate, and α-methoxy-α-trifluoromethylphenylacetate (MTPA) esters. J Am
Chem Soc 95:512
75. Theil F, Costisella B, Schick H (1992) A correlation of configuration and 19 F-NMR chemical
shifts of (R)-(+)-Mosher esters of chiral cyclopentanediol derivatives. J Prakt Chem 334:85
76. Bhilabutra W, Techowisan T, Peberdy JF, Lumyong S (2007) Antimicrobial activity of
bioactive compounds from Periconia siamensis CMUGE015. Res J Microbiol 2:749
77. Fun H-K, Bhilabutra W, Tuntiwachwuttikul P, Chantrapromma S (2006) 5,8-Dihydroxy-10methyl-5,8,9,10-tetrahydro-2H-oxecin-2-one. Acta Cryst E 62:o2478
78. Evidente A, Cimmino A, Berestetskiy A, Andolfi A, Motta A (2008) Stagonolides G−I and
modiolide A, nonenolides produced by Stagonospora cirsii, a potential mycoherbicide for
Cirsium arvense. J Nat Prod 71:1897
79. Greve H, Schupp PJ, Eguereva E, Kehraus S, König GM (2008) Ten-membered lactones from
the marine-derived fungus Curvularia sp. J Nat Prod 71:1651
80. Mondol MAM, Farthouse J, Islam MT, Schüffler A, Laatsch H (2017) Metabolites from the
endophytic fungus Curvularia sp. M12 act as motility inhibitors against Phytophthora capsici
zoospores. J Nat Prod 80:347
81. Zheng C-J, Shao C-L, Chen M, Niu Z-G, Zhao D-L, Wang C-Y (2015) Merosesquiterpenoids and ten-membered macrolides from a soft coral-derived Lophiostoma sp. fungus.
Chem Biodivers 12:1407
82. Quang TH, Kim DC, Van Kiem P, Van Minh C, Nhiem NX, Tai BH, Yen PH, Thi Thanh
Ngan N, Kim HJ, Oh H (2018) Macrolide and phenolic metabolites from the marine-derived
fungus Paraconiothyrium sp. VK-13 with anti-inflammatory activity. J Antibiot 71:826
83. Pescitelli G (2018) For a correct application of the CD exciton chirality method: the case of
laucysteinamide A. Mar Drugs 16:388
84. Matsuda M, Yamazaki T, Fuhshuku K-I, Sugai T (2007) First total synthesis of modiolide
A, based on the whole-cell yeast-catalyzed asymmetric reduction of a propargyl ketone.
Tetrahedron 63:8752
85. Gil A, Albericio F, Álvarez M (2017) Role of the Nozaki–Hiyama–Takai–Kishi reaction in
the synthesis of natural products. Chem Rev 117:8420
86. Mohapatra DK, Dash U, Naidu PR, Yadav JS (2009) Stereoselective total synthesis of
stagonolide C and formal total synthesis of modiolide A. Synlett 2129
87. Yuzikhin O, Mitina G, Berestetskiy A (2007) Herbicidal potential of stagonolide, a new
phytotoxic nonenolide from Stagonospora cirsii. J Agric Food Chem 55:7707
88. Berestetskiy A, Dmitriev A, Mitina G, Lisker I, Andolfi A, Evidente A (2008) Nonenolides
and cytochalasins with phytotoxic activity against Cirsium arvense and Sonchus arvensis: a
structure–activity relationships study. Phytochemistry 69:953
89. Evidente A, Cimmino A, Berestetskiy A, Mitina G, Andolfi A, Motta A (2008) Stagonolides
B–F, nonenolides produced by Stagonospora cirsii, a potential mycoherbicide of Cirsium
arvense. J Nat Prod 71:31
90. Dalinova A, Dubovik V, Chisty L, Kochura D, Ivanov A, Smirnov S, Petrova M, Zolotarev
A, Evidente A, Berestetskiy A (2019) Stagonolides J and K and stagochromene A, two new
natural substituted nonenolides and a new disubstituted chromene-4,5-dione isolated from
Stagonospora cirsii S-47 proposed for the biocontrol of Sonchus arvensis. J Agric Food
Chem 67:13040
91. Rivero-Cruz JF, García-Aguirre G, Cerda-García-Rojas CM, Mata R (2000) Conformational
behavior and absolute stereostructure of two phytotoxic nonenolides from the fungus Phoma
herbarum. Tetrahedron 56:5337