Unknown

Dataset Information

0

1-[4-(2,3,4,6-Tetra-O-acetyl-?-d-allo-pyranos-yloxy)benzyl-idene]thio-semi-carbazide.


ABSTRACT: The title compound, C(22)H(27)N(3)O(10)S, was synthesized by reaction of an ethanol solution of helicid (systematic name: 4-formylphenl-?-d-allopyranoside), thio-semicarbazide and acetic acid. The mol-ecule exhibits a trans conformation with respect to the C=N double bond. The pyran ring adopts a chair conformation. In the crystal structure, the mol-ecules are linked into chains parallel to the b axis by inter-molecular N-H?O hydrogen bonds.

SUBMITTER: Fu L 

PROVIDER: S-EPMC2968846 | biostudies-other | 2009

REPOSITORIES: biostudies-other

altmetric image

Publications

1-[4-(2,3,4,6-Tetra-O-acetyl-β-d-allo-pyranos-yloxy)benzyl-idene]thio-semi-carbazide.

Fu Li L   Yin Xiu-Juan XJ   Zheng Lei L   Li Ying Y   Yin Shu-Fan SF  

Acta crystallographica. Section E, Structure reports online 20090306 Pt 4


The title compound, C(22)H(27)N(3)O(10)S, was synthesized by reaction of an ethanol solution of helicid (systematic name: 4-formylphenl-β-d-allopyranoside), thio-semicarbazide and acetic acid. The mol-ecule exhibits a trans conformation with respect to the C=N double bond. The pyran ring adopts a chair conformation. In the crystal structure, the mol-ecules are linked into chains parallel to the b axis by inter-molecular N-H⋯O hydrogen bonds. ...[more]

Similar Datasets

| S-EPMC3052038 | biostudies-literature
| S-EPMC2983542 | biostudies-literature
| S-EPMC4011224 | biostudies-literature
| S-EPMC4719930 | biostudies-literature
| S-EPMC2979748 | biostudies-literature
| S-EPMC3050357 | biostudies-literature
| S-EPMC2983406 | biostudies-literature
| S-EPMC2979487 | biostudies-literature
| S-EPMC2915049 | biostudies-literature
| S-EPMC2959596 | biostudies-literature