✦ LIBER ✦

Haem d1: development of a new coupling procedure leading to the synthesis of isobacteriochlorins 1

✍ Scribed by Mackman, Richard L.; Micklefield, Jason; Block, Michael H.; Leeper, Finian J.; Battersby, Alan R.

Book ID: 121375513
Publisher: Royal Society of Chemistry
Year: 1997
Weight: 179 KB
Volume: 14
Category: Article
ISSN: 1472-7781
DOI: 10.1039/A700654C

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Haem d1: Developmen

ChemInform Abstract: Haem d1: Development of a New Coupling Procedure Leading to the Synthesis of Isobacteriochlorins.

✍ R. L. MACKMAN; J. MICKLEFIELD; M. H. BLOCK; F. J. LEEPER; A. R. BATTERSBY 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

A new Procedure for the Synthesis of (E)

A new Procedure for the Synthesis of (E)-1-iodo-1-alkenes.

✍ A.García Martínez; R.Martínez Alvarez; S.Martínez González; L.R. Subramanian; M. 📂 Article 📅 1992 🏛 Elsevier Science 🌐 French ⚖ 136 KB

ChemInform Abstract: Haem d1: Stereosele

ChemInform Abstract: Haem d1: Stereoselective Synthesis of the Reduced Form of Its Parent Macrocycle Using the Original Coupling Strategy.

✍ C. J. AUCKEN; F. J. LEEPER; A. R. BATTERSBY 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB

A feature of reaction of 1,1′-diacetylfe

A feature of reaction of 1,1′-diacetylferrocene with dimethylformamide dimethyl acetal leading to a new strategy of the synthesis of asymmetrical 1,1′-disubstituted ferrocene

✍ A. I. Moskalenko; A. V. Boeva; V. I. Boev 📂 Article 📅 2011 🏛 Springer 🌐 English ⚖ 172 KB

Synthesis of spiro-substituted 1,3-oxazi

Synthesis of spiro-substituted 1,3-oxazines by a new sequence leading to spiroheterocycles

✍ L. Fišera; F. Sauter; J. Fröhlich; Y. Feng; K. Mereiter 📂 Article 📅 1994 🏛 Springer Vienna 🌐 English ⚖ 594 KB

N-Alkylation-coupling reaction of imines

N-Alkylation-coupling reaction of imines promoted by alkylaluminum reagents, leading to a facile synthesis of 1,2-diamines

✍ Makoto Shimizu; Yasuki Niwa 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 67 KB

N-Alkylation-coupling reactions of the imines derived from glyoxylate esters were conducted with dialkylaluminum chloride in acetonitrile to give N-monoalkylated 1,2-diamines in good yields.