cheminform abstract: the vitamin c route to the ciguatoxins: enantioselective synthesis of a ring f...

2000 other bioactive products other bioactive products U 1300 31 - 238 The Vitamin C Route to the Ciguatoxins: Enantioselective Synthesis of a Ring F Building Block. — Key steps of the described total synthesis are a ring closure metathesis/oxidative cleavage sequence to form the nine-membered ring and two highly diastereoselective reductions. — (BOND, SILAS; PERLMUTTER, PATRICK; Chem. Commun. (Cambridge) (2000) 7, 567-568; Dep. Chem., Monash Univ., Clayton, Victoria 3168, Australia; EN) 1

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Page 1: ChemInform Abstract: The Vitamin C Route to the Ciguatoxins: Enantioselective Synthesis of a Ring F Building Block

2000 other bioactive products

other bioactive productsU 1300

31 - 238The Vitamin C Route to the Ciguatoxins: Enantioselective Synthesisof a Ring F Building Block. — Key steps of the described totalsynthesis are a ring closure metathesis/oxidative cleavage sequence to form thenine-membered ring and two highly diastereoselective reductions. — (BOND,SILAS; PERLMUTTER, PATRICK; Chem. Commun. (Cambridge) (2000) 7,567-568; Dep. Chem., Monash Univ., Clayton, Victoria 3168, Australia; EN)

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