Process for the preparation of thienamycin and intermediates

In a process for the total synthesis of thienamycin from L-aspartic acid via intermediate III: III R=H, blocking group or salt cation there is disclosed a process for preparing III via wherein R is a protecting group.

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Bibliographic Details
Main Authors RATCLIFFE; RONALD W, CHRISTENSEN; BURTON G, SALZMANN; THOMAS N
Format Patent
LanguageEnglish
Published 09.09.1986
Edition4
Subjects
ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
CHEMISTRY
CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION ORPROCESSING OF GOODS
GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINSTCLIMATE CHANGE
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Summary:In a process for the total synthesis of thienamycin from L-aspartic acid via intermediate III: III R=H, blocking group or salt cation there is disclosed a process for preparing III via wherein R is a protecting group.
Bibliography:Application Number: US19850786366