Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一些全酶是高度复杂的，如丙酮酸氢酶。

Citral was synthesized by catalytical rearrangement of dehydrolinalool in toluene solution with the present of molybdenyl acetylacetonate, benzoic acid and dimethyl sulfoxide (DMSO).

摘要氢芳樟醇为原料，在乙酰丙酮酸钼、苯甲酸、二甲基亚砜(DMSO)的甲苯溶液中催化重排合成柠檬醛，考察了柠檬醛在不同体系中的热性。

In working skeletal muscle under anaerobic conditions, glyceraldehyde 3-phosphate is converted to pyruvate (the payoff phase of glycolysis), and the pyruvate is reduced to lactate .

骨骼肌在厌氧条件下工作，3-磷酸甘油醛转变成丙酮酸(糖酵解的收获阶段)，丙酮酸又转变成乳酸。

It reports the synthsis of a new low toxic organic sulphur germicide pyruvoyl - hydrazono - 1, 3 - ditholane.The stracture of objective compound was identified and determined.

报道了一种新型、低毒的有菌剂——丙酮酸缩肼叉-1，3-二噻茂烷的合成，并对目标化合物的结构进行了分析。

Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一些全酶是高度复杂的，如丙氢酶。

Citral was synthesized by catalytical rearrangement of dehydrolinalool in toluene solution with the present of molybdenyl acetylacetonate, benzoic acid and dimethyl sulfoxide (DMSO).

摘要采用氢芳樟醇为原料，在乙酰丙钼、苯甲、二甲基亚砜(DMSO)的甲苯溶液中催化重排合成柠檬醛，考察了柠檬醛在不同体系中的热性。

In working skeletal muscle under anaerobic conditions, glyceraldehyde 3-phosphate is converted to pyruvate (the payoff phase of glycolysis), and the pyruvate is reduced to lactate .

骨骼肌在厌氧条件下工作，3-磷甘油醛转变成丙(糖酵解的收获阶段)，丙又转变成乳。

It reports the synthsis of a new low toxic organic sulphur germicide pyruvoyl - hydrazono - 1, 3 - ditholane.The stracture of objective compound was identified and determined.

报道了一种新型、低毒的有机硫杀菌剂——丙叉-1，3-二噻茂烷的合成，并对目标化合物的结构进行了分析。

Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一些全酶是高度复杂的，如丙酮酸脱氢酶。

Citral was synthesized by catalytical rearrangement of dehydrolinalool in toluene solution with the present of molybdenyl acetylacetonate, benzoic acid and dimethyl sulfoxide (DMSO).

摘要采用脱氢芳原料，在乙酰丙酮酸钼、苯甲酸、二甲基亚砜(DMSO)的甲苯溶液中催化重排合成柠檬醛，考察了柠檬醛在不同体系中的热性。

In working skeletal muscle under anaerobic conditions, glyceraldehyde 3-phosphate is converted to pyruvate (the payoff phase of glycolysis), and the pyruvate is reduced to lactate .

骨骼肌在厌氧条件下工作，3-磷酸甘油醛转变成丙酮酸(糖酵解的收获阶段)，丙酮酸又转变成乳酸。

It reports the synthsis of a new low toxic organic sulphur germicide pyruvoyl - hydrazono - 1, 3 - ditholane.The stracture of objective compound was identified and determined.

报道了一种新、的有机硫杀菌剂——丙酮酸缩肼叉-1，3-二噻茂烷的合成，并对目标化合物的结构进行了分析。

Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一些全酶是高度复杂的，如丙酮酸脱氢酶。

Citral was synthesized by catalytical rearrangement of dehydrolinalool in toluene solution with the present of molybdenyl acetylacetonate, benzoic acid and dimethyl sulfoxide (DMSO).

摘要采用脱氢芳樟醇为原料，在乙酰丙酮酸钼、苯甲酸、二甲基亚砜(DMSO)的甲苯溶液中催化重排合成柠檬醛，考察了柠檬醛在不同体系中的热性。

In working skeletal muscle under anaerobic conditions, glyceraldehyde 3-phosphate is converted to pyruvate (the payoff phase of glycolysis), and the pyruvate is reduced to lactate .

骨骼肌在厌氧条件下工作，3-磷酸甘油醛转变成丙酮酸(糖酵解的收获阶段)，丙酮酸又转变成乳酸。

It reports the synthsis of a new low toxic organic sulphur germicide pyruvoyl - hydrazono - 1, 3 - ditholane.The stracture of objective compound was identified and determined.

报道了一种新型、低毒的有机硫杀菌剂——丙酮酸缩肼叉-1，3-二噻茂烷的合成，并对目标化合物的结构进行了。

Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一些全酶是高度复杂的，如脱氢酶。

Citral was synthesized by catalytical rearrangement of dehydrolinalool in toluene solution with the present of molybdenyl acetylacetonate, benzoic acid and dimethyl sulfoxide (DMSO).

摘要采用脱氢芳樟醇为原料，在乙酰钼、苯、亚砜(DMSO)的苯溶液中催化重排合成柠檬醛，考察了柠檬醛在不同体系中的热性。

In working skeletal muscle under anaerobic conditions, glyceraldehyde 3-phosphate is converted to pyruvate (the payoff phase of glycolysis), and the pyruvate is reduced to lactate .

骨骼肌在厌氧条件下工作，3-磷甘油醛转变成(糖酵解的收获阶段)，又转变成乳。

It reports the synthsis of a new low toxic organic sulphur germicide pyruvoyl - hydrazono - 1, 3 - ditholane.The stracture of objective compound was identified and determined.

报道了一种新型、低毒的有机硫杀菌剂——缩肼叉-1，3-噻茂烷的合成，并对目标化合物的结构进行了分析。

Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一些全酶是高度复杂，如丙酮酸脱氢酶。

Citral was synthesized by catalytical rearrangement of dehydrolinalool in toluene solution with the present of molybdenyl acetylacetonate, benzoic acid and dimethyl sulfoxide (DMSO).

摘要采用脱氢芳樟醇为原料，在乙酰丙酮酸钼、酸、二基亚砜(DMSO)溶液中催化重排合成柠檬醛，考察了柠檬醛在不同体系中热性。

In working skeletal muscle under anaerobic conditions, glyceraldehyde 3-phosphate is converted to pyruvate (the payoff phase of glycolysis), and the pyruvate is reduced to lactate .

骨骼肌在厌氧条件下工作，3-磷酸甘油醛转变成丙酮酸(糖酵解阶段)，丙酮酸又转变成乳酸。

It reports the synthsis of a new low toxic organic sulphur germicide pyruvoyl - hydrazono - 1, 3 - ditholane.The stracture of objective compound was identified and determined.

报道了一种新型、低毒有机硫杀菌剂——丙酮酸缩肼叉-1，3-二噻茂烷合成，并对目标化合物结构进行了分析。

Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一些全酶是高度复杂，如丙酮酸脱酶。

Citral was synthesized by catalytical rearrangement of dehydrolinalool in toluene solution with the present of molybdenyl acetylacetonate, benzoic acid and dimethyl sulfoxide (DMSO).

摘要采用脱醇为原料，在乙酰丙酮酸钼、苯甲酸、二甲基亚砜(DMSO)甲苯溶液中催化重排合成柠檬醛，考察了柠檬醛在不同体系中热性。

In working skeletal muscle under anaerobic conditions, glyceraldehyde 3-phosphate is converted to pyruvate (the payoff phase of glycolysis), and the pyruvate is reduced to lactate .

骨骼肌在厌氧条件下工作，3-磷酸甘油醛转变成丙酮酸(糖酵解收获阶段)，丙酮酸又转变成乳酸。

It reports the synthsis of a new low toxic organic sulphur germicide pyruvoyl - hydrazono - 1, 3 - ditholane.The stracture of objective compound was identified and determined.

报道了一种新型、低有机硫杀菌剂——丙酮酸缩肼叉-1，3-二噻茂烷合成，并对目标化合物结构进行了分析。

Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一些全酶是高度，如丙酮酸脱氢酶。

Citral was synthesized by catalytical rearrangement of dehydrolinalool in toluene solution with the present of molybdenyl acetylacetonate, benzoic acid and dimethyl sulfoxide (DMSO).

摘要采用脱氢芳樟醇为原料，在乙酰丙酮酸钼、苯甲酸、二甲基亚砜(DMSO)甲苯溶液中催化重排合成柠檬醛，考察了柠檬醛在不同体系中热性。

In working skeletal muscle under anaerobic conditions, glyceraldehyde 3-phosphate is converted to pyruvate (the payoff phase of glycolysis), and the pyruvate is reduced to lactate .

骨骼肌在厌氧条件下工作，3-磷酸甘油醛转变成丙酮酸(糖酵解收获阶段)，丙酮酸又转变成乳酸。

It reports the synthsis of a new low toxic organic sulphur germicide pyruvoyl - hydrazono - 1, 3 - ditholane.The stracture of objective compound was identified and determined.

报道了一种新型、低毒有机硫杀菌剂——丙酮酸缩肼叉-1，3-二合成，并对目标化合物结构进行了分析。

Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一些全酶是高度复杂的，如丙酮酸脱氢酶。

Citral was synthesized by catalytical rearrangement of dehydrolinalool in toluene solution with the present of molybdenyl acetylacetonate, benzoic acid and dimethyl sulfoxide (DMSO).

摘要采用脱氢芳樟醇为原料，在乙酰丙酮酸钼、苯甲酸、二甲基亚砜(DMSO)的甲苯溶液中催化重排合成，考察了在不同体系中的热性。

In working skeletal muscle under anaerobic conditions, glyceraldehyde 3-phosphate is converted to pyruvate (the payoff phase of glycolysis), and the pyruvate is reduced to lactate .

骨骼肌在厌氧条件作，3-磷酸甘油转变成丙酮酸(糖酵解的收获阶段)，丙酮酸又转变成乳酸。

It reports the synthsis of a new low toxic organic sulphur germicide pyruvoyl - hydrazono - 1, 3 - ditholane.The stracture of objective compound was identified and determined.

报道了一种新型、低毒的有机硫杀菌剂——丙酮酸缩肼叉-1，3-二噻茂烷的合成，并对目标化合物的结构进行了分析。

Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一些全酶是高度复杂的，如丙酮酸脱氢酶。

Citral was synthesized by catalytical rearrangement of dehydrolinalool in toluene solution with the present of molybdenyl acetylacetonate, benzoic acid and dimethyl sulfoxide (DMSO).

摘要采用脱氢芳樟醇为原料，在乙酰丙酮酸钼、苯甲酸、二甲基亚砜(DMSO)的甲苯溶液中催化重排合成，考察了在不同体系中的热性。

In working skeletal muscle under anaerobic conditions, glyceraldehyde 3-phosphate is converted to pyruvate (the payoff phase of glycolysis), and the pyruvate is reduced to lactate .

骨骼肌在厌氧条件下工作，3-磷酸转变成丙酮酸(糖酵解的收获阶段)，丙酮酸又转变成乳酸。

It reports the synthsis of a new low toxic organic sulphur germicide pyruvoyl - hydrazono - 1, 3 - ditholane.The stracture of objective compound was identified and determined.

报道了一种新型、低毒的有机硫杀菌剂——丙酮酸缩肼叉-1，3-二噻茂烷的合成，并对目标化合物的结构进行了分析。