Biologically active glycosides from Asteroidea. XV: Asymmetric synthesis of phytosphingosine and phytosphingosine anhydro base: assignment of the absolute stereochemistry
- Author
- SUGIYAMA, S1 ; HONDA, M; KOMORI, T
[1] Kyushu univ., fac. pharmaceutical sci., Higashi-ku Fukuoka 812, Japan - Source
Liebigs Annalen der Chemie. 1988, Num 7, pp 619-625 ; ref : 16 ref
- CODEN
- LACHDL
- ISSN
- 0170-2041
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- VCH, Weinheim
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aminoalcool Aminoglycoside Composé aliphatique Composé saturé Cycle 5 chaînons Dédoublement optique Epoxydation Hydrocarbure bromé Hétérocycle oxygène Stéréochimie Synthèse asymétrique Triol Dodécane(bromo-«1») Furannol-3(amino-«4» lauryl-«2» perhydro) Hexadécanetriol-1,3,4(amino-2)
- Keyword (en)
- Aminoalcohol Aminoglycoside Aliphatic compound Saturated compound Five membered ring Optical resolution Epoxidation Bromocarbon Oxygen heterocycle Stereochemistry Asymmetric synthesis Triol
- Keyword (es)
- Aminoalcohol Aminoglicósido Compuesto alifático Compuesto saturado Ciclo 5 eslabones Desdoblamiento óptico Epoxidación Hidrocarburo bromado Heterociclo oxígeno Estereoquímica Síntesis asimétrica Triol
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C07 Carbohydrates. Nucleosides and nucleotides / 001C03C07A Carbohydrates with 4, 5, 6, ... C atoms, dissacharides and oligosaccharides
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 7223869
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1002/jlac.198819880702 
https://dx.doi.org/10.1002/jlac.198819880702
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