A Contribution to the Asymmetric Synthesis of 3‐Amino β‐Lactams: The Diastereoselective [2+2] Cycloaddition Reaction of Chiral Aminoketene Equivalents with Enolizable Aldehyde‐Derived Imines
1997; Wiley; Volume: 3; Issue: 9 Linguagem: Inglês
10.1002/chem.19970030909
ISSN1521-3765
AutoresClaudio Palomo, J. M. Aizpurua, Marta Legido, Antonia Mielgo, Regina Galarza,
Tópico(s)Synthesis and Catalytic Reactions
ResumoAbstract N ‐[Bis(trimethylsilyl)methyl]imines 9 show unique chemical properties when compared with conventional imines. Their reaction with optically pure aminoketenes derived from dehydrochlorination of 14 and 15 affords the corresponding 3‐amino‐4‐alkyl‐β‐lactams 16 and 17 in good yields and high diastereoselectivities. The mild deprotection of bis(trimethylsilyl)methyl‐ and phenyloxazolidinone moieties with, respectively, cerium(IV) ammonium nitrate and lithium/ammonia or hydrogen/Pd(OH) 2 allows the preparation of a variety of β‐lactam antibiotic building blocks.
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