所有图片(1)
About This Item
经验公式（希尔记法）:
C15H13NO2
CAS号:
分子量:
239.27
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22
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化驗
98%
光學活性
[α]23/D −57±4°, c = 2 in chloroform (or methanol)
mp
227-232 °C (lit.)
官能基
phenyl
SMILES 字串
O=C1N[C@H]([C@H](O1)c2ccccc2)c3ccccc3
InChI
1S/C15H13NO2/c17-15-16-13(11-7-3-1-4-8-11)14(18-15)12-9-5-2-6-10-12/h1-10,13-14H,(H,16,17)/t13-,14+/m0/s1
InChI 密鑰
LTENIVFVXMCOQI-UONOGXRCSA-N
應用
多功能手性助剂，用于各种高非对映选择性反应，例如 Michael 加成反应、Diels-Alder 反应、环丙烷化反应和烯丙基化反应。
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Davies, I.W. et al.
Tetrahedron Letters, 36, 7619-7619 (1995)
Arun K. Ghosh et al.
The Journal of organic chemistry, 61(18), 6175-6182 (1996-09-06)
Sinefungin (1) a nucleoside antibiotic isolated from Streptomyces has been synthesized from D-ribose. Both the C-6 and C-9 stereogenic centers were constructed by efficient asymmetric syntheses. The C-6 amine stereochemistry was set by a highly diastereoselective allylation (>99% de) of
Akiba, T. et al.
Tetrahedron, 50, 3905-3905 (1994)
Davies, S.G. Sanganee, H.J.
Tetrahedron Asymmetry, 6, 671-671 (1995)
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