The stereoselective total synthesis of (−)-cleistenolide is described employing the Barbier allylation, MacMillan α-hydroxylation, Stille-Gennari olefination, and CeCl<SUB>3</SUB>·7H<SUB>2</SUB>O mediated lactonization as key steps
This thesis describes the total syntheses of the sesterterpenoid (±)-palauolide (55) and the diterpe...
148 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1987.The product stereoselectivity...
A convergent and flexible synthetic route for the synthesis of C3–C12 fragment of iriomoteolide-1a i...
A facile stereoselective total synthesis of cleistenolide (1) from the natural chiral template D-ara...
A modulable tin based allylation method for the synthesis of 1,2,3-triols is described. The optimiza...
Polyhydroxylated fragments are ubiquitous in natural products possessing interesting biological prop...
The total synthesis of (−)-ecklonialactone B as well as the 9,10-dihydro derivative by two different...
Cleistanthol of the diterpenoid group is a newly isolated naturally-occuring molecule of biological ...
An efficient, stereoselective synthesis of 4′-Ed4T is demonstrated. The synthesis is highlighted by ...
A simple strategy has been developed for the synthesis of both enantiomers of nor-canadensolide, epi...
A total synthesis of racemic β -necrodol is described using an ortho-ester claisen rearrangement as ...
An approach to the total synthesis of the 14-membered macrolide antibiotic aglycon chlorothricolide ...
A stereoselective synthesis of crinosterol, (22E,24S)-ergosta-5,22-dien- 3\u3b2-ol, was developed fr...
The first part of the dissertation describes the total synthesis of the polyketide marine natural pr...
A stereoselective synthesis of (±)-veadeiroic acid (x) and (±)-veadeirol (XI), diterpenes with cleis...
This thesis describes the total syntheses of the sesterterpenoid (±)-palauolide (55) and the diterpe...
148 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1987.The product stereoselectivity...
A convergent and flexible synthetic route for the synthesis of C3–C12 fragment of iriomoteolide-1a i...
A facile stereoselective total synthesis of cleistenolide (1) from the natural chiral template D-ara...
A modulable tin based allylation method for the synthesis of 1,2,3-triols is described. The optimiza...
Polyhydroxylated fragments are ubiquitous in natural products possessing interesting biological prop...
The total synthesis of (−)-ecklonialactone B as well as the 9,10-dihydro derivative by two different...
Cleistanthol of the diterpenoid group is a newly isolated naturally-occuring molecule of biological ...
An efficient, stereoselective synthesis of 4′-Ed4T is demonstrated. The synthesis is highlighted by ...
A simple strategy has been developed for the synthesis of both enantiomers of nor-canadensolide, epi...
A total synthesis of racemic β -necrodol is described using an ortho-ester claisen rearrangement as ...
An approach to the total synthesis of the 14-membered macrolide antibiotic aglycon chlorothricolide ...
A stereoselective synthesis of crinosterol, (22E,24S)-ergosta-5,22-dien- 3\u3b2-ol, was developed fr...
The first part of the dissertation describes the total synthesis of the polyketide marine natural pr...
A stereoselective synthesis of (±)-veadeiroic acid (x) and (±)-veadeirol (XI), diterpenes with cleis...
This thesis describes the total syntheses of the sesterterpenoid (±)-palauolide (55) and the diterpe...
148 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1987.The product stereoselectivity...
A convergent and flexible synthetic route for the synthesis of C3–C12 fragment of iriomoteolide-1a i...
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