One of the oldest and most useful reactions in organic chemistry is the Fischer indole synthesis (FIS). It is known to have a wide variety of applications including the synthesis of indole rings, often present as the framework in the total synthesis of natural products, particularly those found in the realm of alkaloids, which comprise a ring system known as an indole alkaloid. In this review, we are trying to emphasize the applications of FIS as an old reaction, which is currently applied to the total synthesis of biologically active natural products and some other complex targets
University of Minnesota Ph.D. dissertation.December 2016. Major: Chemistry. Advisor: Wayland Noland...
140 Years ago Adolf von Baeyer proposed the structure of a heteroaromatic compound which revolutioni...
Functionalized indoles are synthezised under mild conditions in a tartaric acid–dimethylurea melt. T...
Indole Compounds have been prepared With good yields using Fischer syntheses in three different meth...
Chapter one provides an overview of the history of the akuammiline alkaloids, includingtheir isolati...
Chapter one discusses previous synthetic efforts toward the communesin alkaloids and perophoramidine...
We developed an environmentally friendly mechanochemical protocol to induce an effective Fischer ind...
Indole terpenoids comprise a large class of natural products with diverse structural topologies and ...
Chapter one discusses the previous use of synthetic chemistry in biosynthetic studies of natural pro...
This dissertation encompasses several projects pertaining to natural product total synthesis, reacti...
International audienceWe developed an environmentally friendly mechanochemical protocol to induce an...
A new one-pot version of the titled reaction involves heating a mixture of a carbonyl compound, a ph...
Development of novel synthetic methodologies and their application to synthesis of natural products ...
Aryl hydrazides with a ketone or aldehyde containing side chains linked to the meta-position of the ...
Functionalized indoles are synthezised under mild conditions in a tartaric acid-dimethylurea melt. T...
University of Minnesota Ph.D. dissertation.December 2016. Major: Chemistry. Advisor: Wayland Noland...
140 Years ago Adolf von Baeyer proposed the structure of a heteroaromatic compound which revolutioni...
Functionalized indoles are synthezised under mild conditions in a tartaric acid–dimethylurea melt. T...
Indole Compounds have been prepared With good yields using Fischer syntheses in three different meth...
Chapter one provides an overview of the history of the akuammiline alkaloids, includingtheir isolati...
Chapter one discusses previous synthetic efforts toward the communesin alkaloids and perophoramidine...
We developed an environmentally friendly mechanochemical protocol to induce an effective Fischer ind...
Indole terpenoids comprise a large class of natural products with diverse structural topologies and ...
Chapter one discusses the previous use of synthetic chemistry in biosynthetic studies of natural pro...
This dissertation encompasses several projects pertaining to natural product total synthesis, reacti...
International audienceWe developed an environmentally friendly mechanochemical protocol to induce an...
A new one-pot version of the titled reaction involves heating a mixture of a carbonyl compound, a ph...
Development of novel synthetic methodologies and their application to synthesis of natural products ...
Aryl hydrazides with a ketone or aldehyde containing side chains linked to the meta-position of the ...
Functionalized indoles are synthezised under mild conditions in a tartaric acid-dimethylurea melt. T...
University of Minnesota Ph.D. dissertation.December 2016. Major: Chemistry. Advisor: Wayland Noland...
140 Years ago Adolf von Baeyer proposed the structure of a heteroaromatic compound which revolutioni...
Functionalized indoles are synthezised under mild conditions in a tartaric acid–dimethylurea melt. T...