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Recent Developments in the Catalytic, Asymmetric Construction of Pyrroloindolines Bearing All-Carbon Quaternary Stereocenters
Pyrroloindoline alkaloids constitute a large family of natural products that has inspired the development of an impressive array of new reactions to prepare the key heterocyclic motif. This synopsis will address catalytic, asymmetric reactions developed to synthesize pyrroloindolines bearing C3a all...
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Published in: | Journal of organic chemistry 2013-12, Vol.78 (24), p.12314-12320 |
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container_title | Journal of organic chemistry |
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creator | Repka, Lindsay M Reisman, Sarah E |
description | Pyrroloindoline alkaloids constitute a large family of natural products that has inspired the development of an impressive array of new reactions to prepare the key heterocyclic motif. This synopsis will address catalytic, asymmetric reactions developed to synthesize pyrroloindolines bearing C3a all-carbon quaternary stereocenters. The methods described herein include both transition-metal-catalyzed and organocatalyzed reactions that have been demonstrated to be suitable for the synthesis of the pyrroloindoline framework. |
doi_str_mv | 10.1021/jo4017953 |
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subjects | alkaloids Carbon - chemistry Catalysis chemical reactions chemical structure Indoles - chemical synthesis Indoles - chemistry Molecular Structure organic chemistry Organometallic Compounds - chemistry Pyrroles - chemical synthesis Pyrroles - chemistry Stereoisomerism Transition Elements - chemistry |
title | Recent Developments in the Catalytic, Asymmetric Construction of Pyrroloindolines Bearing All-Carbon Quaternary Stereocenters |
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