HRID192238

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID640

1-(2-Deoxypentofuranosyl)pyrimidine-2,4(1H,3H)-dione

C9H12N2O5

HCID1049

Pyridine

C5H5N

HCID6456

Trityl chloride

C19H15Cl

PRODUCTS

生成物

结构：O=c1ccn(C2CC(O)C(COC(c3ccccc3)(c3ccccc3)c3ccccc3)O2)c(=O)[nH]1

HCID341822

MLS003171338

C28H26N2O5

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-1a36c9a435214ceebe7fd8ec3f58f9dd
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (6/10)

反应 SMILES

[C:17]([c:18]1[cH:19][cH:20][cH:21][cH:22][cH:23]1)([c:24]1[cH:25][cH:26][cH:27][cH:28][cH:29]1)([c:30]1[cH:31][cH:32][cH:33][cH:34][cH:35]1)[Cl:36].[OH:1][CH2:2][CH:3]1[O:4][CH:5]([n:9]2[cH:10][cH:11][c:12](=[O:13])[nH:14][c:15]2=[O:16])[CH2:6][CH:7]1[OH:8].[cH:37]1[cH:38][cH:39][n:40][cH:41][cH:42]1>>[O:1]([CH2:2][CH:3]1[O:4][CH:5]([n:9]2[cH:10][cH:11][c:12](=[O:13])[nH:14][c:15]2=[O:16])[CH2:6][CH:7]1[OH:8])[C:17]([c:18]1[cH:19][cH:20][cH:21][cH:22][cH:23]1)([c:24]1[cH:25][cH:26][cH:27][cH:28][cH:29]1)[c:30]1[cH:31][cH:32][cH:33][cH:34][cH:35]1