Literature DB >> 27598827

A Mild and General Larock Indolization Protocol for the Preparation of Unnatural Tryptophans.

Kangway V Chuang1, Madeleine E Kieffer1, Sarah E Reisman1.   

Abstract

A mild and general protocol for the Pd(0)-catalyzed heteroannulation of o-bromoanilines and alkynes is described. Application of a Pd(0)/P((t)Bu)3 catalyst system enables the efficient coupling of o-bromoanilines at 60 °C, mitigating deleterious side reactions and enabling access to a broad range of useful unnatural tryptophans. The utility of this new protocol is demonstrated in the highly convergent total synthesis of the bisindole natural product (-)-aspergilazine A.

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Year:  2016        PMID: 27598827      PMCID: PMC5505074          DOI: 10.1021/acs.orglett.6b02477

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  30 in total

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5.  Efficient asymmetric synthesis of tryptophan analogues having useful photophysical properties.

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8.  A new entry to polycyclic indole skeletons via palladium-catalyzed intramolecular heteroannulation.

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9.  Azatryptophans endow proteins with intrinsic blue fluorescence.

Authors:  Sandra Lepthien; Michael G Hoesl; Lars Merkel; Nediljko Budisa
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4.  Structure and Function of NzeB, a Versatile C-C and C-N Bond-Forming Diketopiperazine Dimerase.

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5.  Synthesis of 5-Cyano-Tryptophan as a Two-Dimensional Infrared Spectroscopic Reporter of Structure.

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6.  Access to N-unprotected 2-amide-substituted indoles from Ugi adducts via palladium-catalyzed intramolecular cyclization of o-iodoanilines bearing furan rings.

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  6 in total

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