Volume 21, Issue 37
Organoelement Compounds
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ChemInform Abstract: Intramolecular Amine Coordination versus NMe C-H Activation: The Stereoselective Synthesis of a Tantala(V)azacyclopropane Complex.

H. C. L. ABBENHUIS

H. C. L. ABBENHUIS

Dep. Met.-Mediated Synth., Univ. Utrecht, 3584 CH Utrecht

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D. M. GROVE

D. M. GROVE

Dep. Met.-Mediated Synth., Univ. Utrecht, 3584 CH Utrecht

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G. P. M. VAN MIER

G. P. M. VAN MIER

Dep. Met.-Mediated Synth., Univ. Utrecht, 3584 CH Utrecht

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A. L. SPEK

A. L. SPEK

Dep. Met.-Mediated Synth., Univ. Utrecht, 3584 CH Utrecht

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G. VAN KOTEN

G. VAN KOTEN

Dep. Met.-Mediated Synth., Univ. Utrecht, 3584 CH Utrecht

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First published: September 11, 1990

Abstract

A stereoselective C-H activation reaction of a NMe group of the Ta(V) compound (I) affords toluene and the new pentagonal pyramidal Ta(V) THF adduct (III) (space group P1, Z=4).

ChemInform Abstract

A stereoselective C-H activation reaction of a NMe group of the Ta(V) compound (I) affords toluene and the new pentagonal pyramidal Ta(V) THF adduct (III) (space group P1, Z=4). The chirality of the arylamine leads to a single structurally characterized diastereoisomer in which intramolecular coordination of the modified amine group produces a triangular cyclic Ta-CH2-N unit.

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