A one-pot, lynchpin approach to 1,4-disubstituted E,E-butadienes via multiple cyanocuprate-mediated transmetalations
- Author
- LIPSHUTZ, B. H; JAE IN LEE
Univ. California, dep. chemistry, Santa Barbara CA 93106, United States - Source
Tetrahedron letters. 1991, Vol 32, Num 49, pp 7211-7214 ; ref : 6 ref
- CODEN
- TELEAY
- ISSN
- 0040-4039
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Addition Michaël Composé aliphatique Composé diénique conjugué Composé monocyclique Cétone Enone Réaction one pot Stannane organique Transmétallation Buta-1,3-diène(1,4-bis [triméthylstannyl]) Cuivre-dilithium(cyano diméthyl) Cyclohex-2-énone(3-méthyl) Cyclohexanone(3-[5,5-diméthyl-7-oxoocta-1,3-diényl]) Cyclopent-2-énone(3-méthyl) Pent-3-én-2-one(4-méthyl) Etain Composé organique
- Keyword (en)
- Michael addition Aliphatic compound Conjugated dienic compound Monocyclic compound Ketone Enone One pot reaction Organic stannane Transmetalation Tin Organic compounds
- Keyword (es)
- Adición Michael Compuesto alifático Compuesto diénico conjugado Compuesto monocíclico Cetona Enona Reacción one pot Estannano orgánico Transmetalación Estaño Compuesto orgánico
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05A Alicyclic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5101263
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
10.1016/0040-4039(91)80478-O 
https://dx.doi.org/10.1016/0040-4039(91)80478-O
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