ChemInform Abstract: The Synthesis of a Nγ‐Phthalyl‐Nα‐methyl‐α,γ‐diaminobutyryl Congener (Ia) of Virginiamycin S1 (Ib).

Anteunis, M.; Auwera, C. Van Der; Vanfleteren, L.; Borremans, Frans

doi:10.1002/chin.198824344

ChemInform

1988

DOI: 10.1002/chin.198824344

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ChemInform Abstract: The Synthesis of a Nγ‐Phthalyl‐Nα‐methyl‐α,γ‐diaminobutyryl Congener (Ia) of Virginiamycin S1 (Ib).

M. Anteunis¹,

C. Van Der Auwera²,

L. Vanfleteren³

et al.

Abstract: ChemInform Abstract The synthesis of (Ia) is reported using the very efficient coupling agent BOP-Cl (N,N'-bis(3-oxo-2-oxazolidinyl)phosphinic choride) for imino acid peptide bond formation. The total yield is 11% for 5-coupling steps and one lactonization.

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ChemInform Abstract: The Synthesis of a Nγ‐Phthalyl‐Nα‐methyl‐α,γ‐diaminobutyryl Congener (Ia) of Virginiamycin S1 (Ib).

Abstract: ChemInform Abstract The synthesis of (Ia) is reported using the very efficient coupling agent BOP-Cl (N,N'-bis(3-oxo-2-oxazolidinyl)phosphinic choride) for imino acid peptide bond formation. The total yield is 11% for 5-coupling steps and one lactonization.

Cited by 0 publications

References 4 publications

No citations

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