Diacetone glucose architecture as a chirality template. II.1 Versatile synthon for the chiral deuterium labeling and synthesis of all diastereoisomers of chirally monodeuterated glycerol

Katsumi Kakinuma; Yoshihisa Iihama; Izumi Takagi; Kouichi Ozawa; Noriaki Yamauchi; Nobutaka Imamura; Yasuaki Esumi; Masakazu Uramoto

doi:10.1016/S0040-4020(01)92267-7

Diacetone glucose architecture as a chirality template. II.¹ Versatile synthon for the chiral deuterium labeling and synthesis of all diastereoisomers of chirally monodeuterated glycerol

Katsumi Kakinuma, Yoshihisa Iihama, Izumi Takagi, Kouichi Ozawa, Noriaki Yamauchi, Nobutaka Imamura, Yasuaki Esumi, Masakazu Uramoto

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

3 Citations (Scopus)

Abstract

Chirally deuterated ethylene oxide derivatives attached to a diacetone glucose template were developed as new versatile synthons for chiral deuterium labeling. All four diastereoisomers of chirally monodeuterated glycerol were also synthesized by chirality transcription from the same template.

Original language	English
Pages (from-to)	3763-3774
Number of pages	12
Journal	Tetrahedron
Volume	48
Issue number	18
DOIs	https://doi.org/10.1016/S0040-4020(01)92267-7
Publication status	Published - 1992
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4020(01)92267-7

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Kakinuma, K., Iihama, Y., Takagi, I., Ozawa, K., Yamauchi, N., Imamura, N., Esumi, Y., & Uramoto, M. (1992). Diacetone glucose architecture as a chirality template. II.¹ Versatile synthon for the chiral deuterium labeling and synthesis of all diastereoisomers of chirally monodeuterated glycerol. Tetrahedron, 48(18), 3763-3774. https://doi.org/10.1016/S0040-4020(01)92267-7

Diacetone glucose architecture as a chirality template. II.¹ Versatile synthon for the chiral deuterium labeling and synthesis of all diastereoisomers of chirally monodeuterated glycerol. / Kakinuma, Katsumi; Iihama, Yoshihisa; Takagi, Izumi et al.
In: Tetrahedron, Vol. 48, No. 18, 1992, p. 3763-3774.

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

Kakinuma, K, Iihama, Y, Takagi, I, Ozawa, K, Yamauchi, N, Imamura, N, Esumi, Y & Uramoto, M 1992, 'Diacetone glucose architecture as a chirality template. II.¹ Versatile synthon for the chiral deuterium labeling and synthesis of all diastereoisomers of chirally monodeuterated glycerol', Tetrahedron, vol. 48, no. 18, pp. 3763-3774. https://doi.org/10.1016/S0040-4020(01)92267-7

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abstract = "Chirally deuterated ethylene oxide derivatives attached to a diacetone glucose template were developed as new versatile synthons for chiral deuterium labeling. All four diastereoisomers of chirally monodeuterated glycerol were also synthesized by chirality transcription from the same template.",

author = "Katsumi Kakinuma and Yoshihisa Iihama and Izumi Takagi and Kouichi Ozawa and Noriaki Yamauchi and Nobutaka Imamura and Yasuaki Esumi and Masakazu Uramoto",

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AU - Kakinuma, Katsumi

AU - Iihama, Yoshihisa

AU - Takagi, Izumi

AU - Ozawa, Kouichi

AU - Yamauchi, Noriaki

AU - Imamura, Nobutaka

AU - Esumi, Yasuaki

AU - Uramoto, Masakazu

PY - 1992

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Diacetone glucose architecture as a chirality template. II.¹ Versatile synthon for the chiral deuterium labeling and synthesis of all diastereoisomers of chirally monodeuterated glycerol

Abstract

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