50
B. Schmidt
References
1. Naves YR, Grampoloff AV (1942) Etudes sur les matières végétales volatiles XX. Sur la
composition de l’extrait éthéro-pétrolique (essence concrète) de la fleur de jasmin. Helv Chim
Acta 25:1500
2. Demole E, Willhalm B, Stoll M (1964) Propriétés et structure de la cétolactone C 12 H 16 O 3 de
l’essence de jasmin (Jasminum grandiflorum L.). Helv Chim Acta 47:1152
3. Dräger G, Kirschning A, Thiericke R, Zerlin M (1996) Decanolides, 10-membered lactones
of natural origin. Nat Prod Rep 13:365
4. Ishida T, Wada K (1975) A steroid hydroxylase inhibitor, diplodialide A from Diplodia pinea.
J Chem Soc Chem Commun 209
5. Wada K, Ishida T (1976) A new pentaketide, diplodialide D, from Diplodia pinea. J Chem
Soc Chem Commun:340
6. Wada K, Ishida T (1979) A steroid hydroxylase inhibitor, diplodialide-A, and related
metabolites from Diplodia pinea. J Chem Soc Perkin Trans 1:1154
7. Ramanujan V, Kumar CNSSP (2018) Total synthesis of diplodialides C and D. Arkivoc vii:332
8. Katsuki T, Martin VS (1996) The Sharpless epoxidation. Org React 48:1
9. Singh GS, Mollet K, D’hooghe M, De Kimpe N (2013) Epihalohydrins in organic synthesis.
Chem Rev 113:1441
10. Parenty A, Moreu X, Campagne J-M (2006) Macrolactonizations in the total synthesis of
natural products. Chem Rev 106:911
11. Parenty A, Moreau X, Niel G, Campagne JM (2013) Update 1 of: macrolactonizations in the
total synthesis of natural products. Chem Rev 113:1PR1
12. Sun P, Lu S, Ree VT, Krohn K, Li L, Zhang W (2012) Nonanolides of natural origin: structure,
synthesis, and biological activity. Curr Med Chem 19:3417
13. Ishigami K (2009) Synthetic studies of natural 10-membered lactones, mueggelone, microcarpalide, and Sch 642305, which have interesting bioactivities. Biosci Biotechnol Biochem
73:971
14. Inanaga J, Hirata K, Saeki H, Katsuki T, Yamaguchi M (1979) Rapid esterification by means
of mixed anhydride and its application to large-ring lactonization. Bull Chem Soc Jpn 52:1989
15. Ferraz HMC, Longo LS (2007) Bicyclic β-hydroxytetrahydrofurans as precursors of medium
ring keto-lactones. J Org Chem 72:2945
16. Barradas S, Urbano A, Carreño MC (2009) Concise enantioselective synthesis of the tenmembered lactone cephalosporolide G and its C-3 epimer. Chem Eur J 15:9286
17. Song L, Liu Y, Tong R (2013) Cephalosporolide B serving as a versatile synthetic precursor:
asymmetric biomimetic total syntheses of cephalosporolides C, E, F, G, and (4-OMe-)G. Org
Lett 15:5850
18. Yao H, Wang J, Tong R (2017) Recent developments in total syntheses of cephalosporolides,
penisporolides, and ascospiroketals. Chem Rec 17:1109
19. Neises B, Steglich W (1978) Simple method for the esterification of carboxylic acids. Angew
Chem Int Ed Engl 17:522
20. Blakemore PR, Cole WJ, Kocie´ nski PJ, Morley A (1998) A stereoselective synthesis of
trans-1,2-disubstituted alkenes based on the condensation of aldehydes with metallated 1phenyl-1H-tetrazol-5-yl sulfones. Synlett 26
21. Blakemore PR, Milicevic Sephton S, Ciganek E (2018) The Julia-Kocienski olefination. Org
React 95:1
22. Rej RK, Kumar R, Nanda S (2015) Asymmetric synthesis of cytospolides C and D through
successful exploration of stereoselective Julia–Kocienski olefination and Suzuki reaction
followed by macrolactonization. Tetrahedron 71:3185
23. Sherwood AM, Williamson SE, Johnson SN, Yilmaz A, Day VW, Prisinzano TE (2018)
Scalable regioselective and stereoselective synthesis of functionalized (E)-4-iodobut-3-en-1ols: gram-scale total synthesis of fungal decanolides and derivatives. J Org Chem 83:980
24. Sheehan J, Cruickshank P, Boshart G (1961) A convenient synthesis of water-soluble
carbodiimides. J Org Chem 26:2525
B. Schmidt
References
1. Naves YR, Grampoloff AV (1942) Etudes sur les matières végétales volatiles XX. Sur la
composition de l’extrait éthéro-pétrolique (essence concrète) de la fleur de jasmin. Helv Chim
Acta 25:1500
2. Demole E, Willhalm B, Stoll M (1964) Propriétés et structure de la cétolactone C 12 H 16 O 3 de
l’essence de jasmin (Jasminum grandiflorum L.). Helv Chim Acta 47:1152
3. Dräger G, Kirschning A, Thiericke R, Zerlin M (1996) Decanolides, 10-membered lactones
of natural origin. Nat Prod Rep 13:365
4. Ishida T, Wada K (1975) A steroid hydroxylase inhibitor, diplodialide A from Diplodia pinea.
J Chem Soc Chem Commun 209
5. Wada K, Ishida T (1976) A new pentaketide, diplodialide D, from Diplodia pinea. J Chem
Soc Chem Commun:340
6. Wada K, Ishida T (1979) A steroid hydroxylase inhibitor, diplodialide-A, and related
metabolites from Diplodia pinea. J Chem Soc Perkin Trans 1:1154
7. Ramanujan V, Kumar CNSSP (2018) Total synthesis of diplodialides C and D. Arkivoc vii:332
8. Katsuki T, Martin VS (1996) The Sharpless epoxidation. Org React 48:1
9. Singh GS, Mollet K, D’hooghe M, De Kimpe N (2013) Epihalohydrins in organic synthesis.
Chem Rev 113:1441
10. Parenty A, Moreu X, Campagne J-M (2006) Macrolactonizations in the total synthesis of
natural products. Chem Rev 106:911
11. Parenty A, Moreau X, Niel G, Campagne JM (2013) Update 1 of: macrolactonizations in the
total synthesis of natural products. Chem Rev 113:1PR1
12. Sun P, Lu S, Ree VT, Krohn K, Li L, Zhang W (2012) Nonanolides of natural origin: structure,
synthesis, and biological activity. Curr Med Chem 19:3417
13. Ishigami K (2009) Synthetic studies of natural 10-membered lactones, mueggelone, microcarpalide, and Sch 642305, which have interesting bioactivities. Biosci Biotechnol Biochem
73:971
14. Inanaga J, Hirata K, Saeki H, Katsuki T, Yamaguchi M (1979) Rapid esterification by means
of mixed anhydride and its application to large-ring lactonization. Bull Chem Soc Jpn 52:1989
15. Ferraz HMC, Longo LS (2007) Bicyclic β-hydroxytetrahydrofurans as precursors of medium
ring keto-lactones. J Org Chem 72:2945
16. Barradas S, Urbano A, Carreño MC (2009) Concise enantioselective synthesis of the tenmembered lactone cephalosporolide G and its C-3 epimer. Chem Eur J 15:9286
17. Song L, Liu Y, Tong R (2013) Cephalosporolide B serving as a versatile synthetic precursor:
asymmetric biomimetic total syntheses of cephalosporolides C, E, F, G, and (4-OMe-)G. Org
Lett 15:5850
18. Yao H, Wang J, Tong R (2017) Recent developments in total syntheses of cephalosporolides,
penisporolides, and ascospiroketals. Chem Rec 17:1109
19. Neises B, Steglich W (1978) Simple method for the esterification of carboxylic acids. Angew
Chem Int Ed Engl 17:522
20. Blakemore PR, Cole WJ, Kocie´ nski PJ, Morley A (1998) A stereoselective synthesis of
trans-1,2-disubstituted alkenes based on the condensation of aldehydes with metallated 1phenyl-1H-tetrazol-5-yl sulfones. Synlett 26
21. Blakemore PR, Milicevic Sephton S, Ciganek E (2018) The Julia-Kocienski olefination. Org
React 95:1
22. Rej RK, Kumar R, Nanda S (2015) Asymmetric synthesis of cytospolides C and D through
successful exploration of stereoselective Julia–Kocienski olefination and Suzuki reaction
followed by macrolactonization. Tetrahedron 71:3185
23. Sherwood AM, Williamson SE, Johnson SN, Yilmaz A, Day VW, Prisinzano TE (2018)
Scalable regioselective and stereoselective synthesis of functionalized (E)-4-iodobut-3-en-1ols: gram-scale total synthesis of fungal decanolides and derivatives. J Org Chem 83:980
24. Sheehan J, Cruickshank P, Boshart G (1961) A convenient synthesis of water-soluble
carbodiimides. J Org Chem 26:2525