✦ LIBER ✦

General synthetic route to hexaamine macrocycles

✍ Scribed by Martin, Andrea E.; Bulkowski, John E.

Book ID: 120236721
Publisher: American Chemical Society
Year: 1982
Tongue: English
Weight: 572 KB
Volume: 47
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00342a007

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A simplified synthetic route to polyaza

A simplified synthetic route to polyaza macrocycles

✍ Chavez, F.; Sherry, A. D. 📂 Article 📅 1989 🏛 American Chemical Society 🌐 English ⚖ 450 KB

General synthetic routes to tetraaza mac

General synthetic routes to tetraaza macrocycles. Preparation of the corrin inner ring structure

✍ Tang, S. C.; Weinstein, G. N.; Holm, R. H. 📂 Article 📅 1973 🏛 American Chemical Society 🌐 English ⚖ 283 KB

ChemInform Abstract: A New Synthetic Rou

ChemInform Abstract: A New Synthetic Route to Substituted Cyclam Macrocycles.

✍ B. KOENIG; M. PELKA; H. ZIEG; P. G. JONES; I. DIX 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB

General synthetic route to benz[g]isoqui

General synthetic route to benz[g]isoquinolines (2-azaanthracenes)

✍ A. Paul Krapcho; Timothy P. Gilmor 📂 Article 📅 1998 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 465 KB

## Abstract Benzylic zinc reagents add with high regioselectivity to 1‐(phenoxycarbonyl) salts derived from pyridine‐3‐carboxaldehyde (1a) or 3‐acetylpyridine (1b) to yield 1‐(phenoxylcarbonyl)‐4‐benzyl‐1,4‐dihydropyridine‐3‐carboxaldehydes 5a, 5c or ketones 5b, 5d. Aromatizations of these dihydro

A general synthetic route to nanofibers

A general synthetic route to nanofibers of polyaniline derivatives

✍ Tran, Henry D.; Kaner, Richard B. 📂 Article 📅 2006 🏛 Royal Society of Chemistry 🌐 English ⚖ 366 KB

A general synthetic route to 4-substitut

A general synthetic route to 4-substituted-2,2′-bithiophenes

✍ Seth C. Rasmussen; Jason C. Pickens; James E. Hutchison 📂 Article 📅 1997 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 341 KB

## Abstract A new synthetic route to 4‐substituted‐2,2′‐bithiophenes has been developed utilizing 4‐bromo‐2,2′‐bithiophene (1). Formation of the bithienyllithium adduct __via__ halogen‐metal exchange was found to be problematic and resulted in complex mixtures of products. The Grignard reagent of 1