The design, synthesis, and preliminary evaluation of methyl 1,2,8,8a-tetrahydrocyclopropa[c]thieno[3,2- e]indol-4-one-6-carboxylate (CTI) derivatives are detailed representing a single atom change (N to S) embedded in the duocarmycin SA alkylation subuni
The instability of the hydroxylactone E ring represents a critical drawback of camptothecins, becaus...
A robust procedure for the production of [1,2]dithiolo[4,3- b ]indole-3(4 H)-thione analogues using ...
The hitherto unknown 5,6-dihydroxy-3-mercaptoindole (4a) and its 2-carbomethoxy derivative (4b), as ...
The design, synthesis, and evaluation of a predictably more potent analogue of CC-1065 entailing the...
The design, synthesis, and evaluation of a predictably more potent analog of CC-1065 entailing the s...
The synthesis of 1,2,8,8a-tetrahydrocyclopropa[c]pyrrolo[3,2-e]indol-4(5H)-one (CPI), the parent CC-...
The preparation and evaluation of 6 and 7, analogues of the duocarmycins and CC-1065 in which the su...
(+)-CC-1065 and the duocarmycins are potent antitumor natural products which exert their antitumor e...
The duocarmycins are anti-tumour antibiotics that derive their biological activity through sequence-...
An efficient, concise enantioselective total synthesis of the potent antitumor antibiotic (+)-duocar...
The synthesis of an achiral seco-hydroxy-aza-CBI-TMI analog (8) of the duocarmycins is reported. Its...
The synthesis of tetrahydro-cis-cyclopenta[c]tiophene-5-one ethylenketal and its transformation into...
The duocarmycins are potent antitumor agents with potential for use in the development of antibody–d...
This thesis presents the synthesis of several structural analogues of the immunosuppressant compound...
A series of racemic indole C5-O-substituted seco-cyclopropylindole (seco-CI) compounds 1-5 were prep...
The instability of the hydroxylactone E ring represents a critical drawback of camptothecins, becaus...
A robust procedure for the production of [1,2]dithiolo[4,3- b ]indole-3(4 H)-thione analogues using ...
The hitherto unknown 5,6-dihydroxy-3-mercaptoindole (4a) and its 2-carbomethoxy derivative (4b), as ...
The design, synthesis, and evaluation of a predictably more potent analogue of CC-1065 entailing the...
The design, synthesis, and evaluation of a predictably more potent analog of CC-1065 entailing the s...
The synthesis of 1,2,8,8a-tetrahydrocyclopropa[c]pyrrolo[3,2-e]indol-4(5H)-one (CPI), the parent CC-...
The preparation and evaluation of 6 and 7, analogues of the duocarmycins and CC-1065 in which the su...
(+)-CC-1065 and the duocarmycins are potent antitumor natural products which exert their antitumor e...
The duocarmycins are anti-tumour antibiotics that derive their biological activity through sequence-...
An efficient, concise enantioselective total synthesis of the potent antitumor antibiotic (+)-duocar...
The synthesis of an achiral seco-hydroxy-aza-CBI-TMI analog (8) of the duocarmycins is reported. Its...
The synthesis of tetrahydro-cis-cyclopenta[c]tiophene-5-one ethylenketal and its transformation into...
The duocarmycins are potent antitumor agents with potential for use in the development of antibody–d...
This thesis presents the synthesis of several structural analogues of the immunosuppressant compound...
A series of racemic indole C5-O-substituted seco-cyclopropylindole (seco-CI) compounds 1-5 were prep...
The instability of the hydroxylactone E ring represents a critical drawback of camptothecins, becaus...
A robust procedure for the production of [1,2]dithiolo[4,3- b ]indole-3(4 H)-thione analogues using ...
The hitherto unknown 5,6-dihydroxy-3-mercaptoindole (4a) and its 2-carbomethoxy derivative (4b), as ...