SFX by Ex Libris Inc.

Title:	Chemo-, Regio-, and Enantioselective Pd-Catalyzed Allylic Alkylation of Indolocarbazole Pro-aglycons
Source:	Organic Letters [1523-7060] Trost, Barry yr:2002

Basic

Full text

Full text available via American Chemical Society Journals

Year:

Volume:

Issue:

Start Page:

Document delivery

Request document via Library/Bibliothek

Users interested in this article also expressed an interest in the following:
description	1.	Silva, Luiz F. "Synthesis of polyalkylated indoles using a thallium(III)-mediated ring-contraction reaction." Synthesis 24 (2007): 3851-3857.
description	2.	Trost, Barry M. "5H-Oxazol-4-ones as Building Blocks for Asymmetric Synthesis of Î±-Hydroxycarboxylic Acid Derivatives." Journal of the American Chemical Society 126.7 (2004): 1944-1945.
description	3.	NYSTROM, Jan-Erik E. "PALLADIUM-CATALYZED REGIOSELECTIVE ALLYLATION OF 6,6-DIMETHYLFULVENE - A NEW FULVENE SYNTHESIS." Tetrahedron letters 32.39 (1991): 5247-5250.
description	4.	Braun, M. "New developments in stereoselective palladium-catalyzed allylic alkylations of preformed enolates." Synlett 5 (2006): 661-676.
description	5.	Trost, Barry M. "Palladium-catalyzed DYKAT of butadiene mono-epoxide: enantioselective total synthesis of (+)-DMDP, (-)-bulgecinine, and (+)-broussonetine G." Chemistry : a European journal 12.25 (2006): 6607-6620.
description	6.	Trost, B. "Palladium-catalyzed DYKAT of vinyl epoxides: Enantioselective total synthesis and assignment of the configuration of (+)-broussonetine G." Angewandte Chemie (International ed.) 42.48 (2003): 5987-5990.
description	7.	Ibrahem, I. "Direct catalytic intermolecular Î±-allylic alkylation of aldehydes by combination of transition-metal and organocatalysis." Angewandte Chemie (International ed.) 45.12 (2006): 1952-1956.
description	8.	Kalinin, V N. "Pd-catalyzed asymmetric allylation of an o-carborane derivative." Russian Chemical Bulletin 51.3 (2002): 513-516.
description	9.	Thomasen, H. "3′,4′-trans-Linked bicyclic nucleosides locked in S-type conformations." Chemical communications 2002.17 (2002): 1888-1889.
description	10.	Chen, M. "Iridium-Catalyzed Enantioselective Allylic Substitution of Unstabilized Enolates Derived from Î±,Î²-Unsaturated Ketones." Angewandte Chemie (International ed.) 53.33 (2014): 8691-8695.
description	11.	Sugimura, T. "Direct Asymmetric Aldol Reaction of 5H-Oxazol-4-ones with Aldehydes Catalyzed by Chiral Guanidines." Journal of the American Chemical Society 132.18 (2010): 6286-6287.
description	12.	Trost, Barry M. "Palladium-catalyzed asymmetric allylation of prochiral nucleophiles: synthesis of 3-allyl-3-aryl oxindoles." Angewandte Chemie 44.2 (2004): 308-310.
description	13.	HUWE, C. "SYNTHESIS OF NITROGEN-HETEROCYCLES FROM VINYL GLYCINE DERIVATIVES VIA PALLADIUM CATALYSIS." Tetrahedron Letters 35.51 (1994): 9537-9540.
description	14.	Wei, Zhong g. "A short efficient synthesis of (S)-4-amino-5-hexenoic acid [(S)-vigabatrin]." Journal of organic chemistry 58.6 (1993): 1586-1588.
description	15.	Miyabe, H. "Regio- and stereocontrolled palladium- or iridium-catalyzed allylation." Synlett 2005.11 (2005): 1641-1655.
description	16.	Polet, D. "Phosphoramidite ligands in iridium-catalyzed allylic substitution." Chemistry : a European journal 12.13 (2006): 3596-3609.
description	17.	Roy, S. "Convenient synthesis of masked aminoindoles by indium mediated one-pot reductive acylation of 3- and 2-nitroindoles." Heterocycles 70 (2006): 51-56.
description	18.	Matsuo, Jun-ichi I. "One-pot carbon-carbon bond formation at the beta-position of cyclic ketones: oxidative Michael addition with alkyl malonates." Tetrahedron Letters 48.18 (2007): 3155-3158.
description	19.	Kirkham, J. "Asymmetric synthesis of cytotoxic sponge metabolites R-strongylodiols A and B and an analogue." Tetrahedron 61.30 (2005): 7219-7232.
description	20.	Trost, B. "Utilization of molybdenum- and palladium-catalyzed dynamic kinetic asymmetric transformations for the preparation of tertiary and quaternary stereogenic centers: A concise synthesis of tipranavir." Journal of the American Chemical Society 124.48 (2002): 14320-14321.