The Suzuki-Miyaura reaction in the chemical transformations of vindoline

• Autorzy: Ruszkowska J. , Chrobak R. , Zero P. , Maurin J.K. , Szawkalo J. , Czarnocki Z.
• Języki publikacji: EN

Abstrakty

EN

Vindoline and its analogues are important constituents of the Madagascan periwinkle Catharanthus roseus, and some of them are valuable chemotherapy drugs used in treatment for some types of cancer, including leukaemia, lymphoma, breast and lung cancer. The search for semi-synthetic congeners of natural substances is still an important task for organic chemistry. In this communication we report the synthesis of five new vindoline derivatives, 15-(2-methoxyphenyl)vindoline 11, 15-(3-methoxyphenyl)vindoline 12, 15-(2-nitrophenyl)vindoline 13, 15-(3-cyanophenyl)vindoline 15, and 15-(4-cyanophenyl)vindoline 16 using the Suzuki-Miyaura reaction as the key step. X-Ray analysis of compound 16 is also reported

Słowa kluczowe

PL

alkaloid; natural product; bioorganic chemistry; chemotherapy; vindoline; Madagascar periwinkle; Catharanthus roseus; cancer; treatment

• Wydawca: -
• Czasopismo: Acta Biochimica Polonica
• Rocznik: 2007
• Tom: 54
• Numer: 4
• Strony: 857-861
• Opis fizyczny: p.857-861,fig.,ref.

Twórcy

autor

Ruszkowska J.

• Faculty of Chemistry, Warsaw University, Warsaw, Poland

autor

Chrobak R.

autor

Zero P.

autor

Maurin J.K.

autor

Szawkalo J.

autor

Czarnocki Z.

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