HRID1603450

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

HCID19605134

未命名化合物

PRODUCTS

生成物

结构：Cc1c(CO)sc2cn(CC3=C(C(=O)[O-])N4C(=O)[C@H]([C@@H](C)O)[C@H]4[C@H]3C)c[n+]12

HCID178429624

未命名化合物

收率 6.4%

PROCEDURE

实验过程

The same procedure as in Example 1 was repeated except that 135 mg of allyl (1S,5R,6S)-6-[(1R)-1-allyloxycarbonyloxyethyl]-2-hydroxymethyl-1-methyl-1-carbapen-2-em-3-carboxylate and 186 mg of 2-hydroxymethyl-3-methylimidazo[5,1-b]thiazole were used, thereby obtaining 9.3 mg of the title compound.