The present invention includes a method for preparing cyclic alcohols. The method includes a reduction, deprotection, and rearrangement scheme. The present invention further provides a method of preparation of an intermediate useful in the synthesis of compounds that function as inhibitors of the aspartyl protease enzyme of human immunodeficiency virus (HIV).
本发明涉及一种制备环状醇的方法。该方法包括还原、去保护和重排方案。本发明还提供了一种制备中间体的方法,该中间体在合成作为人类免疫缺陷病毒(HIV)
天冬氨酸蛋白酶酶
抑制剂的化合物中发挥作用。