✦ LIBER ✦

Preparation of (S)-(—)-2,4-Dimethyl-4-isopropylcyclopent-2-enone

✍ Scribed by Edwards, J. D.; Ichikawa, Nobutaka

Book ID: 127325529
Publisher: American Chemical Society
Year: 1964
Tongue: English
Weight: 246 KB
Volume: 29
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo01025a518

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Novel preparation of (−)-4-hydroxycycloh

Novel preparation of (−)-4-hydroxycyclohex-2-enone: reaction of 4-hydroxycyclohex-2-enone and 4-hydroxycyclopent-2-enone with some thiols

✍ Jamie F. Bickley; Paul Evans; Alastair Meek; Ben S. Morgan; Stanley M. Roberts 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 192 KB

Direct preparation of 3,4-dichloro-2,-di

Direct preparation of 3,4-dichloro-2,-dimethyl-3-chromenes from 2,2-dimethyl-4-chromanones

✍ F. Campa; J. Coll; A. Messeguer; M.A. Pericás 📂 Article 📅 1979 🏛 Elsevier Science 🌐 French ⚖ 122 KB

Regiospecific preparation of 2-(carbomet

Regiospecific preparation of 2-(carbomethoxy)-4-methylcyclohept-4-enone via the divinylcyclopropane rearrangement

✍ Marino, Joseph P.; Ferro, Michael P. 📂 Article 📅 1981 🏛 American Chemical Society 🌐 English ⚖ 409 KB

Preparation and Grignard reactions of 2-

Preparation and Grignard reactions of 2-benzoyl-4,4-dimethyl-2-oxazoline

✍ Hansen, John F.; Wang, Su. 📂 Article 📅 1976 🏛 American Chemical Society 🌐 English ⚖ 461 KB

An Efficient Synthesis of 4(S)-Hydroxycy

An Efficient Synthesis of 4(S)-Hydroxycyclopent-2-enone

✍ Khanapure, Subhash P.; Najafi, Nahid; Manna, Sukumar; Yang, Jing-Jing; Rokach, J 📂 Article 📅 1995 🏛 American Chemical Society 🌐 English ⚖ 469 KB

Light-Induced Cycloaddition of 2,3-Dihyd

Light-Induced Cycloaddition of 2,3-Dihydro-2,2-dimethyl-4H-thiopyran-4-one (a 4-Thiacyclohex-2-enone) to Alkenes and Dienes

✍ Kerstin Schmidt; Jürgen Kopf; Paul Margaretha 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 German ⚖ 213 KB

## Abstract The reactivity of (thiacyclic)‐2,3‐dihydro‐2,2‐dimethyl‐4__H__‐thiopyran‐4‐one (**1a**) in light‐induced cycloadditions to furan (**F**), acrylonitrile (**AN**), or 2,3‐dimethylbut‐2‐ene (**TME**) is compared to that of (carbocyclic) 5,5‐dimethylcyclohex‐2‐enone (**1b**). Whereas for th