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5 Deoxystrigol Synthesis Essay

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

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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]

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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]

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