An asymmetric synthesis of a key intermediate to 1β-methylcarbapenem antibiotics

DOI: 10.1016/00404-0399(50)1359P-

Source and publish data:

Tetrahedron Letters p. 6713 - 6716 (1995)

Update date:2022-08-17

Topics:: Authors:

Kang Sung, Ho

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Article abstract of DOI:10.1016/00404-0399(50)1359P-

1β-Methylcarbapenem 3 has been enantioselectively synthesized starting from ethoxyethyl ether 8 and methyl (R)-3-iodo-2-methylpropionate via the intramolecular 1,3-dipolar cycloaddition of nitrone 6, in which the requisite chiral centers were settled.

Full text of DOI:10.1016/00404-0399(50)1359P-

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Article Doi

An asymmetric synthesis of a key intermediate to 1β-methylcarbapenem antibiotics

DOI: 10.1016/00404-0399(50)1359P-

Source and publish data:

Authors:

Article abstract of DOI:10.1016/00404-0399(50)1359P-

Full text of DOI:10.1016/00404-0399(50)1359P-

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