Titanium tetrachloride-mediated enantioselective synthesis of trans β-lactones
- Author
- CARDANI, S; DE TOMA, C; GENNARI, C; SCOLASTICO, C
CNR Univ. Milano, cent. studio sostanze organische naturali, dip. chimica organica industriale, 20133 Milano, Italy - Issue title
- Organotitanium reagents in organic chemistry
- Source
Tetrahedron (Oxford. Print). 1992, Vol 48, Num 27, pp 5557-5564 ; ref : 20 ref
- CODEN
- TETRAB
- ISSN
- 0040-4020
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aldolisation Aminoester Carboxamide Cycle 4 chaînons Enantiosélectivité Hétérocycle oxygène Lactone Stéréoisomère trans Titane IV Chlorure Cétène(hexyl) [2-(diméthylamino)-1-phénylpropyl triméthylsilyl] acétal Leucine(N-formyl) ester 4-[3-hexyl-4-oxooxéthan-2-yl] butyle Oxétane-2-valérique acide(3-hexyl-4-oxo) diéthylamide Pent-4-énoïque acide(5-formyl) diéthylamide
- Keyword (en)
- Aldol condensation Aminoester Carboxamide Four membered ring Enantioselectivity Oxygen heterocycle Lactone Trans stereoisomer Titanium IV Chlorides
- Keyword (es)
- Aldolización Aminoester Carboxamida Ciclo 4 eslabones Enantioselectividad Heterociclo oxígeno Lactona Estereoisómero trans Titanio IV Cloruro
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5420146
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
10.1016/0040-4020(92)80006-2 
https://dx.doi.org/10.1016/0040-4020(92)80006-2
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