✦ LIBER ✦

Addition reactions of heterocyclic compounds. Part XXXIX. 2-Phenyl-ethynylpyridine and related pyridines with acetylenic esters

✍ Scribed by Acheson, R. M.; Bridson, J. N.

Book ID: 120997545
Publisher: The Royal Society of Chemistry
Year: 1969
Tongue: English
Weight: 474 KB
Volume: 8
Category: Article
ISSN: 0022-4952
DOI: 10.1039/J39690001143

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Some reactions of pyridines and related

Some reactions of pyridines and related heterocycles with acetylenic esters (review)

✍ R. M. Acheson 📂 Article 📅 1976 🏛 Springer US 🌐 English ⚖ 642 KB

Chemistry of heterocyclic N-oxides and r

Chemistry of heterocyclic N-oxides and related compounds. 10. Reaction of pyridine N-oxide with 4-methyl- and 4-phenyl-substituted hantzsch esters

✍ A. S. Kurbatova; Yu. V. Kurbatov 📂 Article 📅 1979 🏛 Springer US 🌐 English ⚖ 250 KB

ChemInform Abstract: Polycyclic N-Hetero

ChemInform Abstract: Polycyclic N-Heterocyclic Compounds. Part 65. Ring Cleavage Reactions of Fused Furo[2,3-c]isoquinolines and Related Compounds with Various Nucleophiles.

✍ Kensuke Okuda; Hiroshi Deguchi; Takashi Hirota; Kenji Sasaki 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views

Structure of products from reactions of

Structure of products from reactions of phosphorus pentachloride with phenyl salicylate and 2-hydroxybenzophenone; related compounds. p31 N.M.R. and chemical studies

✍ A. G. Pinkus; P. G. Waldrep; S. Y. Ma 📂 Article 📅 1965 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 627 KB

New Synthetic Technology for the Rapid C

New Synthetic Technology for the Rapid Construction of Novel Heterocycles—Part 2. The Reaction of IBX with Anilides and Related Compounds

✍ K. C. Nicolaou; Yong-Li Zhong; Phil S. Baran 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 111 KB 👁 2 views

New Synthetic Technology for the Rapid C

New Synthetic Technology for the Rapid Construction of Novel Heterocycles—Part 2. The Reaction of IBX with Anilides and Related Compounds

✍ K. C. Nicolaou; Yong-Li Zhong; Phil S. Baran 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 111 KB 👁 2 views

## Experimental Section DMP (2.0 equiv) was added in one portion to a solution of 7 a (0.1 mmol) in benzene (4 mL) or BTF. [6] The solution was heated at reflux (or at 80 ± 85 8C for the reactions in BTF) for about 30 min at which point TLC indicated complete consumption of starting material. Dilu