✦ LIBER ✦

Macromolecular derivatives of N,N-di-(2-chloroethyl)-4-phenylenediamine mustard. 1. Synthesis and in vitro hydrolytic stability

✍ Scribed by Heidi Soyez; Etienne Schacht

Book ID: 114163193
Publisher: Elsevier Science
Year: 1997
Tongue: English
Weight: 645 KB
Volume: 45
Category: Article
ISSN: 0168-3659
DOI: 10.1016/s0168-3659(96)01570-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Macromolecular derivatives of N,N-di-(2-

Macromolecular derivatives of N,N-di-(2-chloroethyl)-4-phenylene diamine mustard. 2. In vitro cytotoxicity and in vivo anticancer efficacy

✍ Heidi Soyez; Leonard W. Seymour; Etienne Schacht 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 198 KB

Synthesis of n, n- di- (β-chloroethyl) d

Synthesis of n, n- di- (β-chloroethyl) derivatives of 1, 5-diamino-1, 2, 3, 4-tetrahydronaphthalene

✍ G. V. Shishkin; V. P. Mamaev; R. M. Latushkina 📂 Article 📅 1968 🏛 Springer 🌐 English ⚖ 184 KB

Synthesis and pesticidal activity of N,N

Synthesis and pesticidal activity of N,N′-diacyl derivatives of 4-chloro-1,2-phenylenediamine

✍ L. V. Molchanov; A. T. Ayupova; Ch. Sh. Kadyrov; V. A. Shapkin 📂 Article 📅 1983 🏛 Springer 🌐 English ⚖ 242 KB

Synthesis, Crystal Structure and in vitr

Synthesis, Crystal Structure and in vitro Antitumor Activity of Di-n-butyltin p-[N, N-Bis(2-chloroethyl)amino]benzoates

✍ Zhong-Wei Zhang; Tao Jiang; Su-Mei Ren; Yan-Xia Zhang; Jing-Sheng Yu 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 119 KB 👁 2 views

Synthesis and antibacterial activity of

Synthesis and antibacterial activity of certain N-acyl-N',N'-di(2-chloroethyl)-N"-(1-oxyl-2,2,6,6-tetramethylpiperidyl-4)-triamides of phosphoric acid

✍ L. D. Protsenko; I. A. Avrutskaya; T. N. Dneprova; E. Yu. Kodintseva; S. M. Andr 📂 Article 📅 1988 🏛 Springer 🌐 English ⚖ 233 KB

Synthesis of new 2H-1,4-thiazines and th

Synthesis of new 2H-1,4-thiazines and their derivatives utilizing N,N-(di-n-alkyl)-N′-arylthiocarbamoylamidines

✍ Moon-Kook Jeon; Kyongtae Kim; Sung Hoon Kim 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 845 KB

The reactions of N,N-(di-n-alkyl)-N'-arylthiocarbamoylamidines (1) with 2-bromo-l-phenylethanone in the presence of K2CO3 in TI-IF at reflux gave 3-(di-n-alkylamino)-2-arylimino-5-phenyl-2H-1,4-thiazines (7) in 32 to 62 % yields. Treatment of compounds 1 with bromoacetyl bromide in the presence of p