Alkylation of 1-(3,4-Disubstituted Phenyl)-2-thioxo-1,2,5,6tetrahydropyrimidin-4(3H)-ones. -Alkylation of the title compounds (I), (VI), and (IX) results in the formation of S-and N-methylated derivatives. S-methylated products (III), (VII), and (X) are always the major products. In all cases, meth
✦ LIBER ✦
cis-4-Carboxy-6-(mercaptomethyl)-3,4,5,6-tetrahydropyrimidin-2(1H)-one, a potent inhibitor of mammalian dihydroorotase
✍ Scribed by Adams, Jerry L.; Meek, Thomas D.; Mong, Shau Ming; Johnson, Randall K.; Metcalf, Brian W.
- Book ID
- 126294439
- Publisher
- American Chemical Society
- Year
- 1988
- Tongue
- English
- Weight
- 772 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0022-2623
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
ChemInform Abstract: Alkylation of 1-(3,
✍
Kristina Kantminiene; Zigmuntas Beresnevicius; Gema Mikulskiene; Jan Kihlberg; J
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 33 KB
👁 1 views
X-ray study of the hetero ring flexibili
✍
S. Stankovic; Á. Kapor; B. Ribár; A. Kálmán; Gy. Argay; L.J. Karanovic; G. Stáje
📂
Article
📅
1985
🏛
Elsevier Science
🌐
English
⚖ 320 KB
Synthesis of 6-(Ethoxymethylenimino)-1,2
✍
Kang-Chien Liu; Ming-Kuan Hu
📂
Article
📅
1987
🏛
John Wiley and Sons
🌐
English
⚖ 128 KB
👁 1 views
5,7-Dihydro-3-[2-[1-(phenylmethyl)-4-pip
✍
Villalobos, Anabella; Butler, Todd W.; Chapin, Douglas S.; Chen, Yuhpyng L.; DeM
📂
Article
📅
1995
🏛
American Chemical Society
🌐
English
⚖ 928 KB
Preparation of 3,4,4a,5,11,11a-Hexahydro
✍
Frank J. Villani; Elizabeth A. Wefer
📂
Article
📅
1970
🏛
Journal of Heterocyclic Chemistry
🌐
English
⚖ 145 KB
A (1,3) Strain in cis- and trans-5, 6-di
✍
Kuppuswamy Nagarajan; Rashmi K. Shah; Hermann Fuhrer; Reginal T. Puckett; Mathur
📂
Article
📅
1978
🏛
John Wiley and Sons
🌐
German
⚖ 611 KB
## Abstract The stereochemistry of __trans__‐ and __cis__‐2, 4‐dimethyl‐tetrahydroquinolines, **6** and **7** were derived from ^1^H‐NMR. studies. These were converted respectively into __trans__‐ and __cis__‐5, 6‐dihydro‐4, 6‐dimethyl‐4__H__, 8__H__‐pyrido [3, 2, 1‐de]phenanthridin‐8‐ones **18** a