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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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