IMPROVED ASYMMETRIC SYNTHESIS OF (-)-3-AMINOCARDICINIC ACID AND FURTHER OBSERVATIONS OF THE MITSUNOBU REACTION FOR β-LACTAM FORMATION IN SERYL PEPTIDES

DOI: 10.1016/S0040-4039(00)85732-9

Source and publish data:

Tetrahedron Letters p. 4859 - 4862 (1982)

Update date:2022-08-04

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Authors:

Townsend, Craig A.

Nguyen, Loan T.

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Article abstract of DOI:10.1016/S0040-4039(00)85732-9

Protected seryl peptide 2 was treated under a variety of conditions with triphenylphosphine or triethylphosphine and diethyl azodicarboxylate to give mechanistic insight into the β-lactam forming reaction and an improved route to (-)-3-aminocardicinic aci

Full text of DOI:10.1016/S0040-4039(00)85732-9

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