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5 Deoxystrigol Synthesis Essay

1. Nicolaou, K. C. &#x; Sorensen E. J. Classics in Total Synthesis: Targets, Strategies, Methods (Wiley, ).

2. Nicolaou, K. C. &#x; Snyder, S. A. Classics in Total Synthesis II: More Targets, Strategies, Methods (Wiley, ).

3. Nicolaou, K. C. &#x; Chen, J. S. Classics in Total Synthesis III (Wiley, ).

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9. Kim HI, et al. Avenaol, a germination stimulant for root parasitic plants from Avena strigosa. Phytochemistry. ;– doi: /dfknj.wz.czhem[PubMed][Cross Ref]

von Salm JL, et al. Shagenes A and B, new tricyclic sesquiterpenes produced by an undescribed antarctic octocoral. Org. Lett. ;– doi: /olx.[PMC free article][PubMed][Cross Ref]

Look SA, Fenical W, Engen DV, Clardy J. Erythrolides: unique marine diterpenoids interrelated by a naturally occurring dfknj.wz.cz-methane rearrangement. J. Am. Chem. Soc. ;– doi: /jaa[Cross Ref]

Cheng Y-B, et al. Nortriterpene lactones from the fruits of Schisandra arisanensis. J. Nat. Prod. ;– doi: /nph.[PubMed][Cross Ref]

Abe S, et al. Carlactone is converted to carlactonoic acid by MAX1 in Arabidopsis and its methyl ester can directly interact with AtD14 in vitro. Proc. Natl Acad. Sci. USA. ;– doi: /pnas[PMC free article][PubMed][Cross Ref]

Yao R, et al. DWARF14 is a non-canonical hormone receptor for strigolactone. Nature. ;– doi: /nature[PubMed][Cross Ref]

Zwanenburg B, Zeljkovic S&#x;, Pospí&#x;il T. Synthesis of strigolactones, a strategic account. Pest Manag. Sci. ;– doi: /ps[PubMed][Cross Ref]

MacAlpine GA, Raphael RA, Shaw A, Taylor AW, Wild H-J. Synthesis of the germination stimulant (±)-strigol. J. Chem. Soc. Chem. Commun. ;– doi: /C[Cross Ref]

Heather JB, Mittal RSD, Sih CJ. Total synthesis of d1-strigol. J. Am. Chem. Soc. ;– doi: /jaa[Cross Ref]

Brooks DW, Bevinakatti HS, Kennedy E, Hathaway J. Practical total synthesis of (+)-strigol. J. Org. Chem. ;– doi: /joa[Cross Ref]

Dailey OD., Jr. A new synthetic route to (+)-Strigol. J. Org. Chem. ;– doi: /joa[Cross Ref]

Hirayama K, Mori K. Synthesis of (+)-strigol and (+)-orobanchol, the germination stimulants, and their stereoisomers by employing lipase-catalyzed asymmetric acetylation as the key step. Eur. J. Org. Chem. ;– doi: /(SICI)() AID-EJOCCO;2-O.[Cross Ref]

Reizelman A, Scheren M, Nefkens GHL, Zwanenburg B. Synthesis of all eight stereoisomers of the germination stimulant strigol. Synthesis. ;– doi: /s[Cross Ref]

Shoji M, Suzuki E, Ueda M. Total synthesis of (±)deoxystrigol via reductive carbon&#x;carbon bond formation. J. Org. Chem. ;– doi: /jo[PubMed][Cross Ref]

Lachia M, Dakas P-Y, De Mesmaeker A. Asymmetric synthesis of the four stereoisomers of 5-deoxystrigol. Tetrahedron Lett. ;– doi: /dfknj.wz.cz[Cross Ref]

Bromhead LJ, Visser J, McErlean CSP. Enantioselective synthesis of the strigolactone mimic (+)-GR J. Org. Chem. ;– doi: /jop.[PubMed][Cross Ref]

Takahashi A, Ogura Y, Enomoto M, Kuwahara S. Enantioselective synthesis of the tricyclic core of (+)-strigol. Tetrahedron. ;– doi: /dfknj.wz.cz[Cross Ref]

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Han Y-X, et al. Biomimetically inspired asymmetric total synthesis of (+)dehydroxyl arisandilactone A. Nat. Commun. ; doi: /ncomms[PMC free article][PubMed][Cross Ref]

Hanessian S, Andreotti D, Gomtsyan A. Asymmetric synthesis of enantiomerically pure and diversely functionalized cyclopropanes. J. Am. Chem. Soc. ;– doi: /jaa[Cross Ref]

Suematsu H, Kanchiku S, Uchida T, Katsuki T. Construction of aryliridium-salen complexes: enantio- and Cis-selective cyclopropanation of conjugated and non-conjugated olefins. J. Am. Chem. Soc. ;– doi: /jat.[PubMed][Cross Ref]

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