𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Facile Synthesis of 2,2-Dimethylchromans by Mo(CO)6-Catalyzed Reaction of Aryl Prenyl Ethers.

✍ Scribed by A. M. BERNARD; M. T. COCCO; V. ONNIS; P. P. PIRAS

Publisher
John Wiley and Sons
Year
2010
Weight
31 KB
Volume
29
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Mo(CO)6-Catalyzed O
ChemInform Abstract: Mo(CO)6-Catalyzed One-Pot Conversion of Allyl Aryl Ethers to Dihydrobenzofurans.
✍ A. M. BERNARD; M. T. COCCO; V. ONNIS; P. P. PIRAS πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 27 KB πŸ‘ 2 views

Mo(CO)6-Catalyzed One-Pot Conversion of Allyl Aryl Ethers to Dihydrobenzofurans. -Mo(CO)6 is found to be an effective catalyst for the tandem Claisen rearrangement-cyclization reaction of the allyl aryl ethers (I) and ( IV) to give dihydrobenzofurans (II) and (V) in good yield. In some cases, trace

ChemInform Abstract: A Facile Synthesis
ChemInform Abstract: A Facile Synthesis of Acetyl-hydroxy-2,2-dimethylchromans and 2,2,-Dimethyl-2H-3,4-dihydropyranoflavanones β€” Dihydro Mixtecacin, Atalantoflavone Dimethyl Ether, and Racemoflavone Dimethyl Ether.
✍ P. E. Kumar; K. J. Rajendra Prasad πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 1 views

A Facile Synthesis of Acetyl-hydroxy-2,2-dimethylchromans and 2,2,-Dimethyl-2H-3,4-dihydropyranoflavanones -Dihydro Mixtecacin, Atalantoflavone Dimethyl Ether, and Racemoflavone Dimethyl Ether. -Thermal Fries rearrangement of chromans (I) and (VI) affords acetyl-hydroxy-chromans such as (II

ChemInform Abstract: Synthesis of Tri- a
ChemInform Abstract: Synthesis of Tri- and Diaryloxybenzenes by Rhodium-Catalyzed Complete Intermolecular [2 + 2 + 2] Cycloaddition of Aryl Ethynyl Ethers.
✍ Yoshiyuki Komine; Yuta Miyauchi; Masayuki Kobayashi; Ken Tanaka πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons βš– 35 KB

## Abstract A cationic Rh(I)‐H~8~‐BINAP complex efficiently catalyzes the cross [2 + 2 + 2] cycloaddition of aryl ethynyl ethers (I) with internal alkynes (II) and homo [2 + 2 + 2] cycloaddition of (I).