𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis, Characterization, and Antibacterial Activity of Complexes of (1S,2S)-N,N-1,2-Diphenylethylene-bis-(5-imino-1-phenyl-1,3-hexanedione)

✍ Scribed by Nasir Ahmad; Nasir Iqbal; Christy Munir

Publisher
Springer Vienna
Year
2000
Tongue
English
Weight
69 KB
Volume
131
Category
Article
ISSN
0026-9247

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of [N-C3H3]-trans-(1R,3S)-(−)-
Synthesis of [N-C3H3]-trans-(1R,3S)-(−)-1-Phenyl-3-N,N-dimethylamino-1,2,3,4-tetrahydronaphthalene (H2-PAT)
✍ Steven D. Wyrick; Andrew M. Myers; Raymond G. Booth; Nora S. Kula; Ross J. Balde 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 French ⚖ 210 KB 👁 1 views

## Abstract Subsequent to the discovery that the (+)‐benzomorphan sigma receptor ligands, (+)‐pentazocine and (+)‐N‐allylnormetazocine, stimulated tyrosine hydroxylase activity and dopamine synthesis in rat striatum __in vitro__, we reported a similar effect on a structurally similar series of 1‐ph

Synthesis and antimicrobial activity of
Synthesis and antimicrobial activity of 3-(N-arylamino)-2-phenyl-naphtho[1,3-d]-1,2-oxaphosphole 2-oxides
✍ P. Haranath; U. Anasuyamma; C. Naga Raju; C. Devendranath Reddy; C. Suresh Reddy 📂 Article 📅 2005 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 97 KB

## Abstract The efficient preparation of __cis__‐3‐(__N__‐arylamino)‐2‐phenylnaphtho[1,3‐__d__]‐1,2‐oxaphosphole 2‐oxides **4** and **5** is described by a three‐component reaction involving phenyldichlorophosphine (**2**) 1‐hydroxy‐2‐naph‐thaldehyde/1‐hydroxy‐2‐acetonaphthone (**1**) and different

Stereoselective synthesis of 2-(S)-(3,5-
Stereoselective synthesis of 2-(S)-(3,5-bis(trifluoromethyl)benzyloxy)-3-(S)-phenyl-1,4-oxazine
✍ Michael S. Ashwood; Ian F. Cottrell; Antony J. Davies 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 370 KB

A convenient process for the preparation of the secondary amine 6, 2-(S)-(3,5-bis(trifluoromethyl)benzyloxy)-3-(S)-phenyl-l,4-oxazine, is described starting from the readily available (S)-phenylglycine 1. The process features efficient construction of the homochiral oxazinone intermediate 3 and ster