Nickel catalyzed imine aldol reactions between activated imines and pronucleophiles

Naomi Shida; Yasufumi Kubota; Hiroyuki Fukui; Naoki Asao; Isao Kadota; Yoshinori Yamamoto

doi:10.1016/00404-0399(50)0912V-

Nickel catalyzed imine aldol reactions between activated imines and pronucleophiles

Naomi Shida, Yasufumi Kubota, Hiroyuki Fukui, Naoki Asao, Isao Kadota, Yoshinori Yamamoto

Research output: Contribution to journal › Article › peer-review

11 Citations (Scopus)

Abstract

Treatment of activated imines 1 with carbonyl compounds 2 in the presence of catalytic amounts of NiCl₂(PPh₃)₂ or NiBr₂(PPh₃)₂ at room temperature affords imine aldol products 3 in high to good yields.

Original language	English
Pages (from-to)	5023-5026
Number of pages	4
Journal	Tetrahedron Letters
Volume	36
Issue number	28
DOIs	https://doi.org/10.1016/00404-0399(50)0912V-
Publication status	Published - Jul 10 1995
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/00404-0399(50)0912V-

Cite this

@article{f214e765a1804970b02d89b61a841959,

title = "Nickel catalyzed imine aldol reactions between activated imines and pronucleophiles",

abstract = "Treatment of activated imines 1 with carbonyl compounds 2 in the presence of catalytic amounts of NiCl2(PPh3)2 or NiBr2(PPh3)2 at room temperature affords imine aldol products 3 in high to good yields.",

author = "Naomi Shida and Yasufumi Kubota and Hiroyuki Fukui and Naoki Asao and Isao Kadota and Yoshinori Yamamoto",

year = "1995",

month = jul,

day = "10",

doi = "10.1016/00404-0399(50)0912V-",

language = "English",

volume = "36",

pages = "5023--5026",

journal = "Tetrahedron Letters",

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publisher = "Elsevier Limited",

number = "28",

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TY - JOUR

T1 - Nickel catalyzed imine aldol reactions between activated imines and pronucleophiles

AU - Shida, Naomi

AU - Kubota, Yasufumi

AU - Fukui, Hiroyuki

AU - Asao, Naoki

AU - Kadota, Isao

AU - Yamamoto, Yoshinori

PY - 1995/7/10

Y1 - 1995/7/10

N2 - Treatment of activated imines 1 with carbonyl compounds 2 in the presence of catalytic amounts of NiCl2(PPh3)2 or NiBr2(PPh3)2 at room temperature affords imine aldol products 3 in high to good yields.

AB - Treatment of activated imines 1 with carbonyl compounds 2 in the presence of catalytic amounts of NiCl2(PPh3)2 or NiBr2(PPh3)2 at room temperature affords imine aldol products 3 in high to good yields.

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U2 - 10.1016/00404-0399(50)0912V-

DO - 10.1016/00404-0399(50)0912V-

M3 - Article

AN - SCOPUS:85047670597

SN - 0040-4039

VL - 36

SP - 5023

EP - 5026

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 28

ER -

Nickel catalyzed imine aldol reactions between activated imines and pronucleophiles

Abstract

ASJC Scopus subject areas

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