stereoselective synthesis of new coumarin and n-methylcarbazole retinoic acid analogues

2004 Vitamins Vitamins U 0900 Stereoselective Synthesis of New Coumarin and N-Methylcarbazole Retinoic Acid Analogues. — [employing Horner—Wadsworth—Emmons olefination reactions of corresponding heterocyclic aldehyde derivatives such as (I), (yields not given)]. — (IVANOVA*, D.; VASSILEVA, M.; VASSILEVA, N.; PASHKULEVA, I.; KOLEVA, R.; J. Indian Chem. Soc. 80 (2003) 6, 650-653; Inst. Genet. Biol. Mol. Cell., F-67401 Illkirch, Fr.; Eng.) — R. Langenstrassen 04- 221

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Page 1: Stereoselective Synthesis of New Coumarin and N-Methylcarbazole Retinoic Acid Analogues

2004 Vitamins

VitaminsU 0900 Stereoselective Synthesis of New Coumarin and N-Methylcarbazole Retinoic Acid

Analogues. — [employing Horner—Wadsworth—Emmons olefination reactions of corresponding heterocyclic aldehyde derivatives such as (I), (yields not given)]. — (IVANOVA*, D.; VASSILEVA, M.; VASSILEVA, N.; PASHKULEVA, I.; KOLEVA, R.; J. Indian Chem. Soc. 80 (2003) 6, 650-653; Inst. Genet. Biol. Mol. Cell., F-67401 Illkirch, Fr.; Eng.) — R. Langenstrassen

04- 221

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