The title compound, C 6 H 12 O 4 , exists in a chair form, with three of the four OH groups equatorially disposed. All four hydroxy groups participate in extensive intermolecular O-HÁ Á ÁO hydrogen bonding.
✦ LIBER ✦
(1R,2R,2′S)-2-(4-Methylphenylsulfonamido)-1-(pyrrolidine-2′-carboxamido)cyclohexane
✍ Scribed by Li, Xinyong ;Chen, Jiarong ;Meng, Xianggao ;Xiao, Wenjing
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 237 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
(1R*,2S*,4S*,5S*)-Cyclohexane-1,2,4,5-
✍
Mehta, Goverdhan ;Sen, Saikat ;Dey, Siddharth
📂
Article
📅
2005
🏛
International Union of Crystallography
🌐
English
⚖ 104 KB
(1S,2S)-2-[(3R,4S)-3-Methyl-4-phenyl-1,2
✍
Ben Ali, Karim ;Chiaroni, Angèle ;Bohe, Luis
📂
Article
📅
2007
🏛
International Union of Crystallography
🌐
English
⚖ 142 KB
(aR,1R,2S,5R)-5-Methyl-2-(1-methyl-1-phe
✍
Wu, Jin-Long
📂
Article
📅
2006
🏛
International Union of Crystallography
🌐
English
⚖ 319 KB
In the molecule of the title compound, C~28~H~42~O~2~, the two cyclohexane rings adopt chair conformations. The olefinic bond and carbonyl group are approximately coplanar.
1′-Methyl-4′-phenylindan-2-spiro-2′-pyr
✍
Selvanayagam, S. ;Devi, M. N. ;Velmurugan, D. ;Ravikumar, K. ;Poornachandran, M.
📂
Article
📅
2006
🏛
International Union of Crystallography
🌐
English
⚖ 170 KB
In the title compound, C 26 H 27 NO 3 , the pyrrolidine ring adopts an envelope conformation. The indanedione group is planar, the dihedral angle between the fused five-and six-membered rings of this group being 1.1 (2) . There are intramolecular C-HÁ Á ÁO and C-HÁ Á Á interactions.
(1R,2R)-N,N′-Bis(4-nitrophenylmethyle
✍
Glidewell, Christopher ;Low, John N. ;Skakle, Janet M. S. ;Wardell, James L.
📂
Article
📅
2005
🏛
International Union of Crystallography
🌐
English
⚖ 192 KB
(2S)-2-[(1R)-1-Iodoethyl]-1-(4-methylp
✍
Kakuda, Hiroko ;Shiro, Motoo
📂
Article
📅
2005
🏛
International Union of Crystallography
🌐
English
⚖ 216 KB