Fast and Highly Regioselective Allylation of Indole and Pyrrole Compounds by Allyl Alcohols Using Ru-Sulfonate Catalysts-Reference-Cited by-同舟云学术

Fast and Highly Regioselective Allylation of Indole and Pyrrole Compounds by Allyl Alcohols Using Ru-Sulfonate Catalysts

Published:2008-08-06 Issue:35 Volume:130 Page:11604-11605
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Zaitsev Alexey B.¹,Gruber Stefan¹,Plüss Pascal A.¹,Pregosin Paul. S.¹,Veiros Luis F.¹,Wörle Michael¹

Affiliation:

1. Laboratory of Inorganic Chemistry, ETHZ, Hönggerberg, CH-8093 Zürich, Switzerland,, Centro de Química Estrutural, Complexo I, Instituto Superior Técnico, 1049-001 Lisbon, Portugal

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja804379k

Reference19 articles.

1. Indole alkaloid marine natural products: An established source of cancer drug leads with considerable promise for the control of parasitic, neurological and other diseases

2. Chemistry and biology of monoterpene indole alkaloid biosynthesis

3. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents

4. Palladium‐Catalysed Cross‐Coupling and Related Reactions Involving Pyrroles

5. Lamellarins and Related Pyrrole-Derived Alkaloids from Marine Organisms

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