The total synthesis of the immunomodulator, (+)-conagenin was achieved using, as a key step, a method developed by us for the synthesis of 2-methyl-1,3-diols via Ti(III)-mediated diastereo- and regioselective opening of trisubstituted 2,3-epoxy alcohols, to carry out the stereoselective construction of its pentanoic acid segment
The first total synthesis of stereochemically pure resolvin D3 and aspirin-triggered resolvin D3 is ...
Development of a unified strategy for the total synthesis of the enmein-type ent-Kauranoids is discl...
A trisubstituted α,β-unsaturated ester moiety was suitably placed in a molecule also bearing an epox...
The total synthesis of the immunomodulator, (+)-conagenin was achieved using, as a key step, a metho...
The total synthesis of stevastelin B3 was achieved using, as a key step, a method developed by us fo...
The formal synthesis of (+)-antimycin A3b and the total synthesis of (+)-blastmycinone were achieved...
An efficient and facile general method for the synthesis of conduritol C analogs, taking advantage o...
The work described herein is a culmination of synthetic studies in the development of a novel method...
The first stereocontrolled total synthesis of iminosugar 1,4-dideoxy-1,4-imino-D-iditol is described...
Polyhydroxylated fragments are ubiquitous in natural products possessing interesting biological prop...
Titanium(IV)-promoted regioselective ring-opening reaction of <i>chiral epoxy–allyl alcohols</i> (S...
The modular synthesis of 1,3-polyols using a chiral phosphine oxide building block is reported. This...
A strategy is outlined for construction of the fungal immunosuppressant FR901483 (1). It was possibl...
The synthesis of the taxanes derivatives has been the major focus of this research. The efforts made...
This work was supported by the Russian Foundation of Basic Research (grant № 15-03-09352 A)
The first total synthesis of stereochemically pure resolvin D3 and aspirin-triggered resolvin D3 is ...
Development of a unified strategy for the total synthesis of the enmein-type ent-Kauranoids is discl...
A trisubstituted α,β-unsaturated ester moiety was suitably placed in a molecule also bearing an epox...
The total synthesis of the immunomodulator, (+)-conagenin was achieved using, as a key step, a metho...
The total synthesis of stevastelin B3 was achieved using, as a key step, a method developed by us fo...
The formal synthesis of (+)-antimycin A3b and the total synthesis of (+)-blastmycinone were achieved...
An efficient and facile general method for the synthesis of conduritol C analogs, taking advantage o...
The work described herein is a culmination of synthetic studies in the development of a novel method...
The first stereocontrolled total synthesis of iminosugar 1,4-dideoxy-1,4-imino-D-iditol is described...
Polyhydroxylated fragments are ubiquitous in natural products possessing interesting biological prop...
Titanium(IV)-promoted regioselective ring-opening reaction of <i>chiral epoxy–allyl alcohols</i> (S...
The modular synthesis of 1,3-polyols using a chiral phosphine oxide building block is reported. This...
A strategy is outlined for construction of the fungal immunosuppressant FR901483 (1). It was possibl...
The synthesis of the taxanes derivatives has been the major focus of this research. The efforts made...
This work was supported by the Russian Foundation of Basic Research (grant № 15-03-09352 A)
The first total synthesis of stereochemically pure resolvin D3 and aspirin-triggered resolvin D3 is ...
Development of a unified strategy for the total synthesis of the enmein-type ent-Kauranoids is discl...
A trisubstituted α,β-unsaturated ester moiety was suitably placed in a molecule also bearing an epox...
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