✦ LIBER ✦

Models for NADH coenzymes. Reactions of 2-carboxyl-substituted pyridines with N-alkyl-1,4-dihydronicotinamides

✍ Scribed by Van Eikeren, Paul; Grier, David L.; Eliason, Jim

Book ID: 126322676
Publisher: American Chemical Society
Year: 1979
Tongue: English
Weight: 493 KB
Volume: 101
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja00518a049

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Enantioselective reduction of CO and C

Enantioselective reduction of CO and CN compounds with NADH model N,N,1,2,4-pentamethyl-1,4-dihydronicotinamide

✍ Jos P. Versleijen; Mireille S. Sanders-Hovens; Sylvia A. Vanhommerig; Jozef A. V 📂 Article 📅 1993 🏛 Elsevier Science 🌐 French ⚖ 747 KB

Stereochemical effects in the reactions

Stereochemical effects in the reactions of n-alkyl-4-substituted azetidine 2-carboxylic acids with oxalyl chloride. Rearrangement to chloro-γ-lactams.

✍ Harry H. Wasserman; William T. Han; John M. Schaus; John W. Faller 📂 Article 📅 1984 🏛 Elsevier Science 🌐 French ⚖ 216 KB

ChemInform Abstract: Reaction of O-Alkyl

ChemInform Abstract: Reaction of O-Alkyl-N-substituted Iminothiocarbonates with Bromoacetyl Bromide. A General Method for the Synthesis of 3-Substituted 1,3- Thiazolidine-2,4-diones.

✍ J. IMRICH; J. BERNAT; P. KRISTIAN; T. BUSOVA; S. HOCOVA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB

Synthesis of [1,2,4]triazolo[3,4-b][1,3]

Synthesis of [1,2,4]triazolo[3,4-b][1,3]thiazine-5-carboxylates via one-pot reaction of N-substituted-hydrazino-carbothioamides with diethyl maleate

✍ Ashraf A. Aly; Alaa A. Hassan; Yusria R. Ibrahim; Mohamed Abdel-Aziz 📂 Article 📅 2009 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 220 KB 👁 1 views

## Abstract magnified image Diethyl maleate reacts with __N__‐substituted‐hydrazino‐carbothioamides to form ethyl [1,2,4]triazolo[3,4‐__b__][1,3]thiazine‐5‐carboxylates. Reaction proceeds __via__ bicyclization and oxidation processes. J. Heterocyclic Chem. (2009).

Studies with polyfunctionally substitute

Studies with polyfunctionally substituted heteroaromatics: A facile route for the synthesis of polyfunctionally substituted N-aminopyridines, 1,2,4-triazolo[1,5-a]pyridines and isoquinolines

✍ Abdel Haleem Mostafa Hussein 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 187 KB 👁 2 views

The reactions of formaldehyde and acetaldehyde with active methylene compounds, followed by reaction with cyanoacetic acid hydrazide 2, afforded N-aminopyridine-2-one derivatives 5a-f. In contrast, the reactions of cyanoacetic acid hydrazide 2 with aliphatic aldehydes and cyanothioacetamide afforded

Reaction of 2-phenyl-2-oxazolin-5-one wi

Reaction of 2-phenyl-2-oxazolin-5-one with 3-N-alkyl/arylisatinimines: One flask synthesis of N-substituted 3-Benzoylamino-2-oxo-1,2-dihydroquinoline-4-carboxamides

✍ Pradeep K. Tripathy; Archana Jain; Arya K. Mukerjee 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 177 KB