A novel method for annulating furans to ketones, involving treatment of the dichlorocarbene adduct of the derived methyl enol ether with base, has been exploited in the synthesis of the title natural product 1 from the known trans-decalone 2. Crow
An organic synthesis ‘round trip’ between natural product total synthesis and the development of new...
An enantioselective synthesis of the macrolactone core of natural product Sch725674 was accomplished...
Two complex norditerpenoids, caribenols A and B, were accessed from a common building block. Our syn...
The core structure of the natural sesquiterpene lactones furanoheliangolides, an 11-oxabicyclo[6.2.1...
It was the purpose of this thesis work to develop new cyclization sequences to be used toward the sy...
A biomimetic synthesis of pallescensin A (1), a furanoid sesquiterpene of natural origin is effected...
The effect of addition of a catalytic quantity of a crown ether in the reaction of a phosphonate ani...
Diels-Alder reaction of 1,3,3-trimethyl-2-vinylcyclohexene I with conjugated ketones 2 - 7 in the pr...
Base-induced elimination of dichlorocarbene adducts 2 to 9-alkoxyphen threnes 1 leads to furans 6, p...
The total synthesis and synthetic efforts towards several diterpene natural products are described. ...
The total synthesis of complex natural products remains one of the enduring challenges in organic ch...
A large number of natural essentially non-terpenoid compounds contain isoprene units. The C<SUB>5</S...
Hyperolactone C is prepared from furan 4. The key transformation is a tandem Claisen rearrangement/l...
Department of Chemistry, Panjab University, Chandigarh-160014 Manuscript received 1 June 1974: acce...
Chapter 1 presents an overview and classification of furan-containing natural products based on skel...
An organic synthesis ‘round trip’ between natural product total synthesis and the development of new...
An enantioselective synthesis of the macrolactone core of natural product Sch725674 was accomplished...
Two complex norditerpenoids, caribenols A and B, were accessed from a common building block. Our syn...
The core structure of the natural sesquiterpene lactones furanoheliangolides, an 11-oxabicyclo[6.2.1...
It was the purpose of this thesis work to develop new cyclization sequences to be used toward the sy...
A biomimetic synthesis of pallescensin A (1), a furanoid sesquiterpene of natural origin is effected...
The effect of addition of a catalytic quantity of a crown ether in the reaction of a phosphonate ani...
Diels-Alder reaction of 1,3,3-trimethyl-2-vinylcyclohexene I with conjugated ketones 2 - 7 in the pr...
Base-induced elimination of dichlorocarbene adducts 2 to 9-alkoxyphen threnes 1 leads to furans 6, p...
The total synthesis and synthetic efforts towards several diterpene natural products are described. ...
The total synthesis of complex natural products remains one of the enduring challenges in organic ch...
A large number of natural essentially non-terpenoid compounds contain isoprene units. The C<SUB>5</S...
Hyperolactone C is prepared from furan 4. The key transformation is a tandem Claisen rearrangement/l...
Department of Chemistry, Panjab University, Chandigarh-160014 Manuscript received 1 June 1974: acce...
Chapter 1 presents an overview and classification of furan-containing natural products based on skel...
An organic synthesis ‘round trip’ between natural product total synthesis and the development of new...
An enantioselective synthesis of the macrolactone core of natural product Sch725674 was accomplished...
Two complex norditerpenoids, caribenols A and B, were accessed from a common building block. Our syn...