HRID1603461

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：C=CCOC(=O)O[C@H](C)[C@H]1C(=O)N2C(C(=O)OCC=C)=C(CO)[C@H](C)[C@H]12

HCID11046746

未命名化合物

HCID19605025

未命名化合物

PRODUCTS

生成物

结构：C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(Cn3cc4scc(CNC=O)[n+]4c3)[C@H](C)[C@H]12

HCID178462302

未命名化合物

收率 1.2%

PROCEDURE

实验过程

The same procedure as in Example 1 was repeated except that 88 mg of allyl (1S,5R,6S)-6-[(1R)-1-allyloxycarbonyloxyethyl]-2-hydroxymethyl-1-methyl-1-carbapen-2-em-3-carboxylate and 70 mg of 3-(formylamino)methylimidazo[5,1-b]thiazole were used, thereby obtaining 1.2 mg of the title compound.