Excellent chiral introduction by diene iron-tricarbonyl moiety .3. Asymmetric synthesis of hydroxyethylidene dipeptide isostere using a diastereoselective 1,2-nucleophilic addition of organocerium reagents into a 1-azatriene Fe(CO)(3) complex
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Takemoto, Y
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OSAKA UNIV, FAC PHARMACEUT SCI, SUITA, OSAKA 565, JAPANOSAKA UNIV, FAC PHARMACEUT SCI, SUITA, OSAKA 565, JAPAN
Takemoto, Y
[1
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Takeuchi, J
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OSAKA UNIV, FAC PHARMACEUT SCI, SUITA, OSAKA 565, JAPANOSAKA UNIV, FAC PHARMACEUT SCI, SUITA, OSAKA 565, JAPAN
Takeuchi, J
[1
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Matsui, E
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OSAKA UNIV, FAC PHARMACEUT SCI, SUITA, OSAKA 565, JAPANOSAKA UNIV, FAC PHARMACEUT SCI, SUITA, OSAKA 565, JAPAN
Matsui, E
[1
]
Iwata, C
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OSAKA UNIV, FAC PHARMACEUT SCI, SUITA, OSAKA 565, JAPANOSAKA UNIV, FAC PHARMACEUT SCI, SUITA, OSAKA 565, JAPAN
Iwata, C
[1
]
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[1] OSAKA UNIV, FAC PHARMACEUT SCI, SUITA, OSAKA 565, JAPAN
A 1-iminobutadiene-iron tricarbonyl [Fe(CO)(3)] complex (1) reacts with various organometallic nucleophiles in a stereoselective manner, and especially, by use of organocerium reagents, only single secondary amine complexes (2) were obtained in good yields. Application of this methodology was demonstrated in the asymmetric synthesis of hydroxyethylidene dipeptide isostere from the chiral starting material N-{(2R)-(2E)-tricarbonyl[2-5-eta-2,4-pentadienylidene]iron} benzylamine (1b).