Results 131 to 140 of about 54,273 (155)
Some of the next articles are maybe not open access.
Journal of the Chemical Society, Perkin Transactions 1, 2001
Diazoketones 1–3, derived from suitably protected amino acids (Ala, Val and Tle), have been photochemically rearranged in the presence of imines leading exclusively to trans-arranged 4-aryl- and cinnamoyl-substituted β-lactams 17–33 with up to 84% yield. Selectivities were dependent on the steric demand of the amino acid side-chain ranging from 65 ∶ 35
Michael R. Linder +2 more
openaire +1 more source
Diazoketones 1–3, derived from suitably protected amino acids (Ala, Val and Tle), have been photochemically rearranged in the presence of imines leading exclusively to trans-arranged 4-aryl- and cinnamoyl-substituted β-lactams 17–33 with up to 84% yield. Selectivities were dependent on the steric demand of the amino acid side-chain ranging from 65 ∶ 35
Michael R. Linder +2 more
openaire +1 more source
Synthesis of 4-aminoguaiazulene and its δ-lactam derivatives
Tetrahedron Letters, 2011Abstract A method for nitrogen insertion into guaiazulene hydrocarbons is developed. A one-pot reaction of 7-isopropyl-1-methylazulene-4-carboxylic acid, diphenylphosphoryl azide, and an alcohol (MeOH, tBuOH or BnOH) affords the corresponding carbamates.
Kiriazis Alexandros +2 more
openaire +1 more source
Proceedings of The 17th International Electronic Conference on Synthetic Organic Chemistry, 2013
The new bifunctional hem-disubstituted alicyclic compounds IIIa-e and IVa-e were synthesized in several steps involving alkylation with allyl bromide following oxidative cleavage. Hem-disubstitues oxo-esters IIIa-e were introduced into azido-Ugi reaction followed by one-pot intramolucular bond formation to afford 3-(tetrazol-5-yl)-2-azaspiro[4.n]alkan ...
Vasiliy Stolyarenko +2 more
openaire +1 more source
The new bifunctional hem-disubstituted alicyclic compounds IIIa-e and IVa-e were synthesized in several steps involving alkylation with allyl bromide following oxidative cleavage. Hem-disubstitues oxo-esters IIIa-e were introduced into azido-Ugi reaction followed by one-pot intramolucular bond formation to afford 3-(tetrazol-5-yl)-2-azaspiro[4.n]alkan ...
Vasiliy Stolyarenko +2 more
openaire +1 more source
Bacterial production of carbapenems and clavams: evolution of β-lactam antibiotic pathways
Trends in Microbiology, 1998Research into two of the four classes of naturally produced beta-lactams--the clavams and carbapenems--has started to throw light upon their biochemical pathways and underlying genetics. Interesting similarities between these two classes, from their joint discovery to an apparently common beta-lactam ring-forming enzyme, are now being revealed.
S J, McGowan, B W, Bycroft, G P, Salmond
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Allergy & Clinical Immunology International - Journal of the World Allergy Organization, 2002
María Sanz, P.M. Gamboa, A.L. de Weck
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María Sanz, P.M. Gamboa, A.L. de Weck
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Structural basis of broad-spectrum β-lactam resistance in Staphylococcus aureus
Nature, 2023J Andrew N Alexander +2 more
exaly
Mn(III)-Promoted Sulfur-Directed 4-Exo-Trig Radical Cyclization of Enamides to β-Lactams
Tetrahedron, 1998openaire +1 more source
Stereoselective construction of β-, γ- and δ-lactam rings via enzymatic C–H amidation
Nature Catalysis, 2023David A Vargas +2 more
exaly
New β-Lactam–β-Lactamase Inhibitor Combinations
Clinical Microbiology Reviews, 2020Dafna Yahav +2 more
exaly

