Addition of aryl substituents to cyclohexadienyliron electrophiles in the development of routes to C12 central building blocks for alkaloid synthesis-Reference-Cited by-同舟云学术

Addition of aryl substituents to cyclohexadienyliron electrophiles in the development of routes to C12 central building blocks for alkaloid synthesis

Published:1999-12 Issue:1 Volume:296 Page:139-149
ISSN:0020-1693
Container-title:Inorganica Chimica Acta
language:en
Short-container-title:Inorganica Chimica Acta

Author:

Malkov Andrej V,Auffrant Audrey,Renard Christophe,Rose Eric,Rose-Munch Françoise,Owen David A,Sandoe Elizabeth J,Richard Stephenson G

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry

Reference18 articles.

1. Advanced Asymmetric Synthesis;Stephenson,1996

2. For example, see Amaryllidaceae alkaloid structures surveyed by S.F. Martin, in: A. Brossi (Ed.), The Alkaloids, Academic Press, 30 (1987) 251; O. Hoshino, in: G.A. Cordell (Ed.), The Alkaloids, 51 (1998) 323.

3. Transition metal mediated asymmetric synthesis, part 151 directing group competition in organoiron intermediates in the synthesis of (±)-O-methyljoubertiamine

4. Switching regiocontrol in 1-aryl-substituted cyclohexadienyliron complexes in a formal total synthesis of lycoramine

5. S.T. Astley, G.R. Stephenson, Synlett, (1992) 507. S.T. Astley, M. Meyer, G.R. Stephenson, Tetrahedron Lett. 34 (1993) 2035.

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5. Electrophilic C12 Building Blocks for Alkaloids: 1,1 Iterative Organoiron-Mediated Routes to (±)-Lycoramine and (±)-Maritidine;European Journal of Organic Chemistry;2011-02-04