A fast, efficient and environmentally benign solvent-free procedure has been developed for microwave-assisted Claisen rearrangement on a silica gel support. Various bis-allyl ketones were prepared using this protocol. (C) 2004 Elsevier Ltd
635-637A rapid, cleaner, cost effective and ecofriendly synthesis of exclusive para aminoaryl keton...
The sol-gel process is a commonly used methodology for producing silica gels with tailored textural ...
Condensations of anhydrides and quinaldine derivatives are accelerated by microwave irradiation unde...
O-Allylsalicylic acids anchored to merrifield resin, are rapidly rearranged to the corresponding ort...
1552-1555Claisen rearrangement of allyl aryl ethers has been studied extensively over various zeoli...
Synthesis of 4,6-diallyl-2-methoxyphenol through Claisen rearrangement of eugenol using microwave ha...
Microwave irradiation, using a commercial microwave oven accelerates (in 10–15 min) the three-step o...
Microwave irradiation, using a commercial microwave oven accelerates (in 10-15 min) the three-step o...
The Claisen rearrangement is a widely applicable organic reaction that involves the shift of a sigma...
A study of microwave-induced and standard thermal Overman rearrangement of selected allylic trichlor...
A convenient synthesis of various aromatic hydroxyketones via Fries rearrangement is described by co...
We demonstrated the rapid Johnson–Claisen rearrangement of allyl alcohol and triethyl orthoacetate w...
ABSTRACT. A one-pot Beckmann rearrangement for the preparation of amides from ketones is described u...
Author Institution: Department of Chemistry, Wesleyan University, 52 Lawn Ave., Middletown, CT 06459...
The Johnson-Claisen rearrangement is a valuable method for the formation of new carbon-carbon bonds,...
635-637A rapid, cleaner, cost effective and ecofriendly synthesis of exclusive para aminoaryl keton...
The sol-gel process is a commonly used methodology for producing silica gels with tailored textural ...
Condensations of anhydrides and quinaldine derivatives are accelerated by microwave irradiation unde...
O-Allylsalicylic acids anchored to merrifield resin, are rapidly rearranged to the corresponding ort...
1552-1555Claisen rearrangement of allyl aryl ethers has been studied extensively over various zeoli...
Synthesis of 4,6-diallyl-2-methoxyphenol through Claisen rearrangement of eugenol using microwave ha...
Microwave irradiation, using a commercial microwave oven accelerates (in 10–15 min) the three-step o...
Microwave irradiation, using a commercial microwave oven accelerates (in 10-15 min) the three-step o...
The Claisen rearrangement is a widely applicable organic reaction that involves the shift of a sigma...
A study of microwave-induced and standard thermal Overman rearrangement of selected allylic trichlor...
A convenient synthesis of various aromatic hydroxyketones via Fries rearrangement is described by co...
We demonstrated the rapid Johnson–Claisen rearrangement of allyl alcohol and triethyl orthoacetate w...
ABSTRACT. A one-pot Beckmann rearrangement for the preparation of amides from ketones is described u...
Author Institution: Department of Chemistry, Wesleyan University, 52 Lawn Ave., Middletown, CT 06459...
The Johnson-Claisen rearrangement is a valuable method for the formation of new carbon-carbon bonds,...
635-637A rapid, cleaner, cost effective and ecofriendly synthesis of exclusive para aminoaryl keton...
The sol-gel process is a commonly used methodology for producing silica gels with tailored textural ...
Condensations of anhydrides and quinaldine derivatives are accelerated by microwave irradiation unde...
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