Total synthesis of hyacinthacines B₃, B₄, and B₅ and purported hyacinthacine B₇, 7-epi-hyacinthacine B₇, and 7a-epi-hyacinthacine B₃ from a common precursor.
نویسندگان
چکیده
The total synthesis of hyacinthacines B3, B4, and B5 and purported hyacinthacine B7, 7-epi-hyacinthacine B7, and 7a-epi-hyacinthacine B3 from a common anti-1,2-amino alcohol precursor is described. These syntheses confirmed that the proposed structures and absolute configurations of hyacinthacines B3, B4, and B5 were correct and disclosed that the proposed structure of hyacinthacine B7 was incorrect. Our synthetic and spectroscopic studies suggest that the natural hyacinthacines B5 and B7 are the same compounds; however, without access to authentic samples this cannot be unequivocally proven.
منابع مشابه
Synthesis of hyacinthacine B3 and purported hyacinthacine B7.
The synthesis of hyacinthacines B(3) and B(7) has confirmed the structure of the former alkaloid and shown that the structure of the latter is incorrect.
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A concise and flexible approach for the asymmetric syntheses of polyhydroxylated pyrrolizidine alkaloids hyacinthacines A(2) and A(3) has been developed using iterative reductive alkylation of O,O'-dibenzyltartarimide (5) as key steps. The ambiguity about the structure of synthetic hyacinthacine A(3) due to the differences in the NMR data of the synthetic material (2) and the natural product (h...
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ورودعنوان ژورنال:
- The Journal of organic chemistry
دوره 79 10 شماره
صفحات -
تاریخ انتشار 2014