✦ LIBER ✦

One-Pot, Catalyst-Free Synthesis of Spirooxindole and 4 H -Pyran Derivatives

✍ Scribed by Ponpandian, Thanasekaran; Muthusubramanian, Shanmugam

Book ID: 125547385
Publisher: Taylor and Francis Group
Year: 2014
Tongue: English
Weight: 296 KB
Volume: 44
Category: Article
ISSN: 0039-7911
DOI: 10.1080/00397911.2013.837488

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Solvent-Free One-Po

ChemInform Abstract: Solvent-Free One-Pot Synthesis of Pyran Derivatives.

✍ Faramarz Rostami-Charati; Zinatossadat Hossaini; Mohammad A. Khalilzadeh; Mahbou 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 18 KB

One-pot synthesis of some 2H-Pyran-2-one

One-pot synthesis of some 2H-Pyran-2-one derivatives

✍ Vladimir Kepe; Marijan Kočevar; Slovenko Polanc 📂 Article 📅 1996 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 268 KB

Solvent-free one-pot synthesis of pyrane

Solvent-free one-pot synthesis of pyrane derivatives

✍ Faramarz Rostami-Charati; Zinatossadat Hossaini; Mohammad A. Khalilzadeh; Mahbou 📂 Article 📅 2011 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 121 KB

One-pot synthesis of polyfunctionalized

One-pot synthesis of polyfunctionalized 4H-pyran derivatives bearing fluorochloro pyridyl moiety

✍ Zhenjun Ye; Renbo Xu; Xusheng Shao; Xiaoyong Xu; Zhong Li 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 409 KB

ChemInform Abstract: An Unique Approach

ChemInform Abstract: An Unique Approach to Catalyst-Free, One-Pot Synthesis of Spirooxindole-Pyrazolines.

✍ Abdolali Alizadeh; Nasrin Zohreh 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 27 KB

One-pot synthesis of functionalized fuse

One-pot synthesis of functionalized fused 4H-pyran systems

✍ Mohammad Bayat; Nader Zabarjad Shiraz; Soheila Shafei Asayesh 📂 Article 📅 2010 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 215 KB

## Abstract magnified image Cyclohexyl isocyanides react with dialkyl acetylenedicarboxylates in the presence of CH‐acids such as cyclohexane‐1,3‐dione or __N,N__′‐dimethylbarbituric acid in one‐pot to afford 4__H__‐pyran annulated heterocyclic systems in fairly high yields. J. Heterocyclic Chem.,