首页> 外国专利> Cyclic triketonforbindelser and trimethylsilyloxybutadienforbindelser and to their use for the preparation of daunomycinonafledede

Cyclic triketonforbindelser and trimethylsilyloxybutadienforbindelser and to their use for the preparation of daunomycinonafledede

机译:环三酮甲酰胺和三甲基甲硅烷氧基丁二烯甲酚及其在制备十二指肠龙胆中的用途

摘要

The invention provides novel cyclic triketone compounds of the formulae CHEM wherein S is H, alkyl or alkoxy and R* is a group of the formule CHEM wherein R1 is methyl and R2 is an alkyl group containing at least 2 carbon atoms, or R1 is an alkyl group having 1-4 carbon atoms and R2 is an aryl group, a hetero aryl group, a -CH2OR min , a -CH2N @@ group, a -CH2SR sec group or a -CH2CH=CH2 group, wherein R min and R sec are alkyl groups having 1-4 carbon atoms. These compounds can be used for preparing daunomycinone and derivatives thereof. Daunomycinone is used for preparing daunomycin and adriamycin. By introducing chirality at C-1 of ring A in the preparation of said novel compounds by using a novel diene of formula (1) in a Diels-Alder reaction for said preparation, the chirality of C-3 is established in the subsequent reaction with LiC IDENTICAL CSi(CH3)3 in the synthesis of daunomycinone and derivatives thereof. CHEM This last reaction leads to the desired compound wherein OH at C-3 and OR at C-1 are in the cis-position with respect to each other.
机译:本发明提供了具有化学式的新型环状三酮化合物,其中S是H,烷基或烷氧基并且R *是式的基团,其中R <1>是甲基并且R2是包含至少2个烷基的烷基碳原子,或R 1为具有1-4个碳原子的烷基,R 2为芳基,杂芳基,-CH2OR min,-CH2N @基,-CH2SR sec基或-CH 2 CH = CH 2基,其中R min和R sec是具有1-4个碳原子的烷基。这些化合物可用于制备道诺霉素及其衍生物。道诺霉素用于制备道诺霉素和阿霉素。通过在用于所述制备的Diels-Alder反应中使用式(1)的新型二烯在所述新型化合物的制备中,在环A的C-1处引入手性,可以在随后的反应中建立C-3的手性。 LiC IDENTICAL CSi(CH3)3在合成道诺霉素及其衍生物中。 该最后反应得到所需的化合物,其中C-3上的OH和C-1上的OR相对于彼此在顺式位置。

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