Literature DB >> 11869135

Rapid route to 3,4-substituted indoles via a directed ortho metalation-retro-Mannich sequence.

Brian Chauder1, Andrew Larkin, Victor Snieckus.   

Abstract

[reaction: see text] In the presence of NXS (X = Br, I, Cl), gramine derivatives 1, derived by combined directed ortho metalation (DoM)-cross-coupling sequences, rapidly undergo retro-Mannich fragmentation (2) to afford 3-halo indoles 3 in 37-88% yields. A conceptually new methodology to diverse 3,4-substituted indoles (10, 11, 13) is thereby introduced.

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Year:  2002        PMID: 11869135     DOI: 10.1021/ol017310m

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


  4 in total

1.  Generation of aza-ortho-xylylenes via ring opening of 2-(2-acylaminophenyl)aziridines: application in the construction of the communesin ring system.

Authors:  Seth L Crawley; Raymond L Funk
Journal:  Org Lett       Date:  2006-08-31       Impact factor: 6.005

2.  Direct organocatalytic coupling of carboxylated piperazine-2,5-diones with indoles through conjugate addition of carbon nucleophiles to indolenine intermediates.

Authors:  Ramin Dubey; Bogdan Olenyuk
Journal:  Tetrahedron Lett       Date:  2010-01-27       Impact factor: 2.415

Review 3.  C4-H indole functionalisation: precedent and prospects.

Authors:  Jagadeesh Kalepu; Parthasarathy Gandeepan; Lutz Ackermann; Lukasz T Pilarski
Journal:  Chem Sci       Date:  2018-04-20       Impact factor: 9.825

4.  Rh2(II)-catalyzed selective aminomethylene migration from styryl azides.

Authors:  Chen Kong; Navendu Jana; Tom G Driver
Journal:  Org Lett       Date:  2013-02-04       Impact factor: 6.005

  4 in total

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