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Total Synthesis of Indole Alkaloids - Based on Direct Construction of Pyrrolocarbazole Scaffolds via Gold-Catalyzed Cascade Cyclizations (Paperback, 1st ed. 2020)
Loot Price: R2,792
Discovery Miles 27 920
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Total Synthesis of Indole Alkaloids - Based on Direct Construction of Pyrrolocarbazole Scaffolds via Gold-Catalyzed Cascade Cyclizations (Paperback, 1st ed. 2020)
Series: Springer Theses
Expected to ship within 10 - 15 working days
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This book explores efficient syntheses of indole alkaloids based on
gold-catalyzed cascade cyclizations, presenting two strategies for
total synthesis of these natural products based on gold-catalyzed
reactions of conjugated diyne or ynamide. The book first describes
the total and formal synthesis of dictyodendrins A-F based on
direct construction of the pyrrolo[2,3-c]carbazole core using the
gold-catalyzed annulation of azido-diynes and protected pyrrole.
This synthetic strategy features late-stage functionalization of
the pyrrolo[2,3-c]carbazole scaffold at several positions and
allows diverse access to dictyodendrins and their derivatives.
Secondly, the book discusses the formal synthesis of vindorosine
based on the pyrrolo[2,3-d]carbazole construction using the
gold-catalyzed cascade cyclization of ynamide. Importantly, the
reaction using a chiral gold complex provides the optically active
pyrrolo[2,3-d]carbazole. This strategy facilitates the rapid
construction of the pyrrolocarbazole core structure of aspidosperma
and related alkaloids, including vindorosine. These methodologies
can accelerate the medicinal application of pyrrolocarbazole-type
alkaloids and related compounds.
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