Herein we report the full details of our efforts toward the application of Pauson-Khand reaction for the stereoselective construction of the trans-decalin subunit with a C16 quaternary stereocenter of fusarisetin A, which led to the asymmetric total synthesis of (+)-fusarisetin A. The developed chemistry provides an alternative strategy to the intramolecular Diels Alder reaction that has been employed for the synthesis of trans-decalin based natural products. (C) 2014 Elsevier Ltd. All rights reserved
The enantioselective synthesis of the fully functionalized BCDE tetracyclic ring system of propindil...
Syntheses of xestodecalactone C and epi-sporostatin are described utilising Prins cyclisations, Mits...
The intermolecular Diels Alder reactions of 5-menthyloxy-2[5H]-furanone with 1-vinylcyclohexenes, 1,...
An asymmetic total synthesis of (+)-fusarisetin A has been achieved. The essential to our strategy w...
An asymmetic total synthesis of (+)-fusarisetin A has been achieved. The essential to our strategy w...
The first total synthesis of (−)-fusarisetin A, the enantiomer of naturally occurring acinar morphog...
A concise, asymmetric total synthesis of (+)-fusarisetin A, a hybrid natural product, has been achie...
A concise, protecting group-free total synthesis of (−)-fusarisetin A (<b>1</b>) was efficiently ach...
A short stereoselective synthesis of the fusarium toxin equisetin, an N-methylserine-derived acyl te...
A concise enantioselective synthesis of (−)-teucvidin has been achieved. Our synthetic strategy invo...
A short stereoselective synthesis of the Fusarium toxin equisetin, a potent inhibitor of HIV-1 integ...
Astellatol and nitidasin belong to a subset of sesterterpenoids that share a sterically encumbered t...
9,10-Substituted cis and trans-decalins were synthesized by a simple route using the Diels-Alder rea...
A concise asymmetric total synthesis of a fusarentin ether (<b>1</b>) with sequential biomimetic tra...
The Co-2(CO)(8)-mediated intramolecular PausonKhand reaction is an efficient approach to the trans-d...
The enantioselective synthesis of the fully functionalized BCDE tetracyclic ring system of propindil...
Syntheses of xestodecalactone C and epi-sporostatin are described utilising Prins cyclisations, Mits...
The intermolecular Diels Alder reactions of 5-menthyloxy-2[5H]-furanone with 1-vinylcyclohexenes, 1,...
An asymmetic total synthesis of (+)-fusarisetin A has been achieved. The essential to our strategy w...
An asymmetic total synthesis of (+)-fusarisetin A has been achieved. The essential to our strategy w...
The first total synthesis of (−)-fusarisetin A, the enantiomer of naturally occurring acinar morphog...
A concise, asymmetric total synthesis of (+)-fusarisetin A, a hybrid natural product, has been achie...
A concise, protecting group-free total synthesis of (−)-fusarisetin A (<b>1</b>) was efficiently ach...
A short stereoselective synthesis of the fusarium toxin equisetin, an N-methylserine-derived acyl te...
A concise enantioselective synthesis of (−)-teucvidin has been achieved. Our synthetic strategy invo...
A short stereoselective synthesis of the Fusarium toxin equisetin, a potent inhibitor of HIV-1 integ...
Astellatol and nitidasin belong to a subset of sesterterpenoids that share a sterically encumbered t...
9,10-Substituted cis and trans-decalins were synthesized by a simple route using the Diels-Alder rea...
A concise asymmetric total synthesis of a fusarentin ether (<b>1</b>) with sequential biomimetic tra...
The Co-2(CO)(8)-mediated intramolecular PausonKhand reaction is an efficient approach to the trans-d...
The enantioselective synthesis of the fully functionalized BCDE tetracyclic ring system of propindil...
Syntheses of xestodecalactone C and epi-sporostatin are described utilising Prins cyclisations, Mits...
The intermolecular Diels Alder reactions of 5-menthyloxy-2[5H]-furanone with 1-vinylcyclohexenes, 1,...