1974
DOI: 10.1021/jo00915a010
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Reactions of pentahapto-cyclohexadienyliron tricarbonyl cations with enamines

Abstract: Bond Angle, deg Bond Angle, deg C(2)-C (1) 1.424 (5) C(2)-C(l)-C(6) 118.3 (3) C (2)-C (1)-F e (23) 67.8 (2) C (6)-C (1) 1.510 (5) C (6)-C (1)-C (16) 114.0 (3) C(6)-C(l)-Fe(23) 109.5 (2) C(16)-C (1)1.512 ( 6) C (16)-C (1)-F e (23)

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Cited by 66 publications
(17 citation statements)
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“…Tricarbonyl(h 5 -cyclohexadienyl)iron(1+) tetrafluoroborate (12), I, and dicarbonyl(h 5 -cyclohexadienyl)(triphenylphosphine)iron(1+) tetrafluoroborate (12), II, were synthesized as described in the literature. 19,20 The salt, I (1.0 g, 3.3 mmol), was dissolved in dry acetonitrile (4 ml) and 3-(diethoxymethylsilyl)propylamine (1.25 g, 6.6 mmol), was added by syringe. The solution was stirred at room temperature for 10 min.…”
Section: Experimental Materials and Synthetic Methodsmentioning
confidence: 99%
“…Tricarbonyl(h 5 -cyclohexadienyl)iron(1+) tetrafluoroborate (12), I, and dicarbonyl(h 5 -cyclohexadienyl)(triphenylphosphine)iron(1+) tetrafluoroborate (12), II, were synthesized as described in the literature. 19,20 The salt, I (1.0 g, 3.3 mmol), was dissolved in dry acetonitrile (4 ml) and 3-(diethoxymethylsilyl)propylamine (1.25 g, 6.6 mmol), was added by syringe. The solution was stirred at room temperature for 10 min.…”
Section: Experimental Materials and Synthetic Methodsmentioning
confidence: 99%
“…The metal will be removed oxidatively under very mild conditions with various reagents to give (7). In particular, metal salts (Fe3+, Cu2+) and trimethylamine N-oxide have been used most successfully (Scheme 4).…”
Section: Methodsmentioning
confidence: 99%
“…Reactions with enolates [6], enamines [7] and allylic silanes [8] in particular should be pointed out, because all these transformations can be done with high chemical yield. No additional Lewis acid is required for reactions with ally1 silanes, which demonstrates the high reactivity of these complexes (Scheme 6).…”
Section: (6) (7) Scheme4mentioning
confidence: 99%
“…O material de partida mais comumente empregado na síntese de estruturas com núcleo octaidroindólico é uma 2-arilcicloexanona, realizando-se adequadamente a funcionalização do intermediário em etapas posteriores. Umezawa e colaboradores utilizaram esta abordagem na preparação de licoranos, como 72, cuja rota sintética encontra-se resumida no Esquema 20(f) 17 .…”
Section: Utilização Das 2-arilcicloexanonas Em Sínteseunclassified