A novel synthesis of cyclic nitrones via a nitrosoketene intermediate

Nobuya Katagiri; Ayumu Kurimoto; Akemi Yamada; Hiroshi Sato; Takao Katsuhara; Koji Takagi; Chikara Kaneko

doi:10.1039/C39940000281

A novel synthesis of cyclic nitrones via a nitrosoketene intermediate

Nobuya Katagiri, Ayumu Kurimoto, Akemi Yamada, Hiroshi Sato, Takao Katsuhara, Koji Takagi, Chikara Kaneko

PHA - Pharmacy

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

5 Citations (Scopus)

Abstract

Nitrosoketene generated by thermolysis of hydroxyimino Meldrum's acid 1 reacts with various ketones including the chiral ketone (+)-nopinone to produce cyclic nitrones 2-5 as novel 1,3-dipolar molecules.

Original language	English
Pages (from-to)	281-282
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	3
DOIs	https://doi.org/10.1039/C39940000281
Publication status	Published - 1994 Dec 1

ASJC Scopus subject areas

Molecular Medicine

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10.1039/C39940000281

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title = "A novel synthesis of cyclic nitrones via a nitrosoketene intermediate",

abstract = "Nitrosoketene generated by thermolysis of hydroxyimino Meldrum's acid 1 reacts with various ketones including the chiral ketone (+)-nopinone to produce cyclic nitrones 2-5 as novel 1,3-dipolar molecules.",

author = "Nobuya Katagiri and Ayumu Kurimoto and Akemi Yamada and Hiroshi Sato and Takao Katsuhara and Koji Takagi and Chikara Kaneko",

year = "1994",

month = dec,

day = "1",

doi = "10.1039/C39940000281",

language = "English",

pages = "281--282",

journal = "Chemical Communications",

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publisher = "Royal Society of Chemistry",

number = "3",

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T1 - A novel synthesis of cyclic nitrones via a nitrosoketene intermediate

AU - Katagiri, Nobuya

AU - Kurimoto, Ayumu

AU - Yamada, Akemi

AU - Sato, Hiroshi

AU - Katsuhara, Takao

AU - Takagi, Koji

AU - Kaneko, Chikara

PY - 1994/12/1

Y1 - 1994/12/1

N2 - Nitrosoketene generated by thermolysis of hydroxyimino Meldrum's acid 1 reacts with various ketones including the chiral ketone (+)-nopinone to produce cyclic nitrones 2-5 as novel 1,3-dipolar molecules.

AB - Nitrosoketene generated by thermolysis of hydroxyimino Meldrum's acid 1 reacts with various ketones including the chiral ketone (+)-nopinone to produce cyclic nitrones 2-5 as novel 1,3-dipolar molecules.

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U2 - 10.1039/C39940000281

DO - 10.1039/C39940000281

M3 - Article

AN - SCOPUS:37049083467

SN - 1359-7345

SP - 281

EP - 282

JO - Chemical Communications

JF - Chemical Communications

IS - 3

ER -

A novel synthesis of cyclic nitrones via a nitrosoketene intermediate

Abstract

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