Pyrrolisoquinoline (B) is found as a major structural motif of the erythrina alkaloid group of natural products. We recognised that a suitably substituted bicyclic lactam (A) could act as a precursor in an intramolecular N-acyliminium mediated cyclisation reaction in a stereoselective approach to the core of the erythrinane target ring system.EThOS - Electronic Theses Online ServiceGBUnited Kingdo
Reaction of β-aminothiols with 2-acylbenzoic acids affords the thiazoloisoindolinones (1) as single ...
For the first time iridium catalysis has been used for the synthesis of chiral tetrahydroisoquinolin...
For the first time iridium catalysis has been used for the synthesis of chiral tetrahydroisoquinolin...
Pyrroloisoquinoline (n = 1) and the pyridoisoquinoline (n = 2) ring systems (2) are found to be the ...
The asymmetric approach to a range of substituted indolizidine templates (3) from nonracemic substra...
Pyrrolisoquinoline (B) is found as a major structural motif of the erythrina alkaloid group of natur...
We describe the application of N-acyliminium cyclisation strategies to access a range of heterocycle...
We describe the application of N-acyliminium cyclisation strategies to access a range of heterocycle...
We describe the application of N-acyliminium cyclisation strategies to access a range of heterocycle...
Pyrrolidinone moieties with a tertiary stereogenic centre at the C-5 position are prevalent in a num...
Novel and complementary routes for the selective preparation of either the 2,11 b-cis (B) or trans (...
Novel and complementary routes for the selective preparation of either the 2,11 b-cis (B) or trans (...
Novel and complementary routes for the selective preparation of either the 2,11 b-cis (B) or trans (...
A formal asymmetric synthesis of both enantiomers of the Erythrina alkaloid 3- demethoxyerythratidin...
The tetracyclic system (219) shares the same heterocyclic skeleton as a plethora of highly bioactive...
Reaction of β-aminothiols with 2-acylbenzoic acids affords the thiazoloisoindolinones (1) as single ...
For the first time iridium catalysis has been used for the synthesis of chiral tetrahydroisoquinolin...
For the first time iridium catalysis has been used for the synthesis of chiral tetrahydroisoquinolin...
Pyrroloisoquinoline (n = 1) and the pyridoisoquinoline (n = 2) ring systems (2) are found to be the ...
The asymmetric approach to a range of substituted indolizidine templates (3) from nonracemic substra...
Pyrrolisoquinoline (B) is found as a major structural motif of the erythrina alkaloid group of natur...
We describe the application of N-acyliminium cyclisation strategies to access a range of heterocycle...
We describe the application of N-acyliminium cyclisation strategies to access a range of heterocycle...
We describe the application of N-acyliminium cyclisation strategies to access a range of heterocycle...
Pyrrolidinone moieties with a tertiary stereogenic centre at the C-5 position are prevalent in a num...
Novel and complementary routes for the selective preparation of either the 2,11 b-cis (B) or trans (...
Novel and complementary routes for the selective preparation of either the 2,11 b-cis (B) or trans (...
Novel and complementary routes for the selective preparation of either the 2,11 b-cis (B) or trans (...
A formal asymmetric synthesis of both enantiomers of the Erythrina alkaloid 3- demethoxyerythratidin...
The tetracyclic system (219) shares the same heterocyclic skeleton as a plethora of highly bioactive...
Reaction of β-aminothiols with 2-acylbenzoic acids affords the thiazoloisoindolinones (1) as single ...
For the first time iridium catalysis has been used for the synthesis of chiral tetrahydroisoquinolin...
For the first time iridium catalysis has been used for the synthesis of chiral tetrahydroisoquinolin...