摘要:
This invention discloses intermediates and a process for the preparation of 6-desmethyl-6-β-hydroxymethyl derivatives of lovastatin and analogs thereof at the 8-acyl side chain.
摘要:
This invention discloses intermediates and a process for the preparation of 6-desmethyl-6-α-hydroxymethyl derivatives of lovastatin and analogs thereof at the 8-acyl side chain.
摘要:
Novel 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors are useful as antihypercholesterolemic agents and are represented by the following general structural formulae (I) and (II):
摘要翻译:新型3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂可用作抗高血胆固醇血症药,并由以下一般结构式(I)和(II)表示: r
摘要:
Novel 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors which are useful as antihypercholesterolemic agents and are represented by the following general structural formulae (I) and (II): and pharmaceutically acceptable salts of the compounds (II) in which Z is hydrogen are disclosed.
摘要:
Novel 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors are useful as antihypercholesterolemic agents and are represented by the following general structural formulae (I) and (II):
摘要翻译:新型3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂可用作抗高血胆固醇血症药,并由以下一般结构式(I)和(II)表示: r
摘要:
This invention discloses intermediates and a process for the preparation of 6-desmethyl-6-carboxy derivatives of lovastatin and analogs thereof at the 8-acyl side chain.
摘要:
Substituted biphenyl-2-carboxaldehydes are prepared in good yield by reacting palladium complexes of substituted benzaldehyde aniline Schiff bases with substituted phenylmagnesium bromides in the presence of at least six, preferably eight, molar equivalents of triphenylphosphine. Those compounds are intermediates for synthetic, in vivo cholesterol synthesis inhibitors.