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Enantioselective cyanoformylation of aldehydes mediated by BINOLAM–AlCl as a monometallic bifunctional catalyst by Jesús Casas; Alejandro Baeza; José M. Sansano; Carmen Nájera; José M. Saá is a Chemistry article available to read on EtoBox.
What is Enantioselective cyanoformylation of aldehydes mediated by BINOLAM–AlCl as a monometallic bifunctional catalyst about?
BINOLAM-AlCl's, binaphthoxide aluminium chloride species generated in situ from either (R)-or (S)-3,3%-bis(diethylaminomethyl)-2,2%-dihydroxy-1,1%-binaphthalene (BINOLAM) behave as Lewis acid-Lewis base (LA-LB) catalysts in the enantioselective addition of methyl cyanoformate to aldehydes at room temperature, thereby leading to the asymmetric synthesis of (S)-or (R)-O-methoxycarbonyl cyanohydrins, respectively.
Who reads Enantioselective cyanoformylation of aldehydes mediated by BINOLAM–AlCl as a monometallic bifunctional catalyst?
It is typically read by researchers, students, and practitioners in Chemistry.
- Author
- Jesús Casas; Alejandro Baeza; José M. Sansano; Carmen Nájera; José M. Saá
- Publisher
- Elsevier Science; Elsevier ; Elsevier Ltd.; Elsevier BV (ISSN 0957-4166)
- Published
- 2003
- Language
- EN
- Field
- Chemistry (Physical Sciences)
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