Stereoconvergent synthesis of the C1-C11 and C12-C24 fragments of (−)-macrolactin-A
- Yadav, J. S.
- Raj Kumar, M.
- Sabitha, G.
DOIAbstract
Stereoconvergent syntheses of the C1-C11 and C12-C24 fragments of (−)-macrolactin-A are reported
Stereoconvergent syntheses of the C1-C11 and C12-C24 fragments of (−)-macrolactin-A are reported
A highly convergent total synthesis of macrolactin A (1) utilizes modern asymmetric catalytic C–C co...
The sponge-derived macrolide (-)-dictyostatin (1) has been reported to exhibit paclitaxel-like effec...
[structures: see text] A short and efficient synthesis of the polyhydroxylated macrolactone (+)-aspi...
A simple and efficient stereoselective synthesis of the C12-C24 fragment of the natural product macr...
The convergent synthesis of the C12-C24 fragment (lower part) of macrolactin A is described. The ad...
A stereoselective synthesis of the C1–C11 fragment of macrolactin A, using original approaches for ...
An enantioselective and convergent synthesis of the C7-C24 fragment of Macrolactin F was achieved fr...
The enantioselective synthesis of the Fe(CO)3 completed C11-C24 segment of macrolactin A has been ac...
A novel, highly convergent, and stereocontrolled synthesis of ($-$)-macrolactin A was accomplished. ...
This dissertation describes synthetic studies culminating in the first total synthesis of the potent...
The C7-C24 tetraene triol segment of macrolactin A was prepared using organoiron chemistry. Two (ca...
The C(19)---C(31) fragment of the anti-tumor macrolide, scytophycin C, was realized in a stereoconve...
Preparation of the Fe(CO)3 complexed C1–C11 and the C16–C24 segments of macrolactin A has been accom...
A unique synthetic strategy towards the natural marine product, Macrolactin A 1, is described. This ...
A synthetic approach towards the cyclic depsipeptide immunosuppressant stevastelin B, based on the s...
A highly convergent total synthesis of macrolactin A (1) utilizes modern asymmetric catalytic C–C co...
The sponge-derived macrolide (-)-dictyostatin (1) has been reported to exhibit paclitaxel-like effec...
[structures: see text] A short and efficient synthesis of the polyhydroxylated macrolactone (+)-aspi...
A simple and efficient stereoselective synthesis of the C12-C24 fragment of the natural product macr...
The convergent synthesis of the C12-C24 fragment (lower part) of macrolactin A is described. The ad...
A stereoselective synthesis of the C1–C11 fragment of macrolactin A, using original approaches for ...
An enantioselective and convergent synthesis of the C7-C24 fragment of Macrolactin F was achieved fr...
The enantioselective synthesis of the Fe(CO)3 completed C11-C24 segment of macrolactin A has been ac...
A novel, highly convergent, and stereocontrolled synthesis of ($-$)-macrolactin A was accomplished. ...
This dissertation describes synthetic studies culminating in the first total synthesis of the potent...
The C7-C24 tetraene triol segment of macrolactin A was prepared using organoiron chemistry. Two (ca...
The C(19)---C(31) fragment of the anti-tumor macrolide, scytophycin C, was realized in a stereoconve...
Preparation of the Fe(CO)3 complexed C1–C11 and the C16–C24 segments of macrolactin A has been accom...
A unique synthetic strategy towards the natural marine product, Macrolactin A 1, is described. This ...
A synthetic approach towards the cyclic depsipeptide immunosuppressant stevastelin B, based on the s...
A highly convergent total synthesis of macrolactin A (1) utilizes modern asymmetric catalytic C–C co...
The sponge-derived macrolide (-)-dictyostatin (1) has been reported to exhibit paclitaxel-like effec...
[structures: see text] A short and efficient synthesis of the polyhydroxylated macrolactone (+)-aspi...
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