As a build-up to the synthesis of the proposed structure of azaspiracid, both enantiomers of fragments 2, 3, and 4 were synthesized stereoselectively. Piv=pivaloyl, PFP=pentafluorophenyl, Teoc=2-(trimethylsilyl)ethoxycarbonyl, TES=triethylsilyl
The previously accepted structure of the marine toxin azaspiracid\u20103 is revised based upon an or...
An efficient synthesis of the C1–C21 fragment of azaspiracids-1 and −3 is described. This features a...
The naturally occurring but scarce marine neurotoxins azaspiracids-1, -2, and -3 have been synthesiz...
As a build-up to the synthesis of the proposed structure of azaspiracid, both enantiomers of fragmen...
Syntheses of the three key building blocks (65, 98, and 100) required for the total synthesis of the...
Syntheses of the three key building blocks (65, 98, and 100) required for the total synthesis of the...
A highly stereoselective and convergent approach for the key intermediate of the FGHI ring system of...
A convergent and stereoselective total synthesis of the previously assigned structure of azaspiracid...
The 39 steps: The recently proposed revised structures of azaspiracid-2 and -3 (see picture), the tw...
An illusive target: The two proposed structures of azaspiracid-1 (1 and FGHI-epi-1), were synthesize...
Graduation date: 2013Azaspiracid-1, a novel marine toxin that contains 9 rings and 20 stereogenic ce...
A convergent and stereoselective total synthesis of the previously assigned structure of azaspiracid...
The key building blocks (6, 7, and 8) for the intended construction of the originally proposed struc...
Access restricted to the OSU CommunityDiscussed herein is the evolution of the strategies for the sy...
A stereoselective synthesis of the ABCD ring framework of azaspiracid-1 and azaspiracid-3 has been a...
The previously accepted structure of the marine toxin azaspiracid\u20103 is revised based upon an or...
An efficient synthesis of the C1–C21 fragment of azaspiracids-1 and −3 is described. This features a...
The naturally occurring but scarce marine neurotoxins azaspiracids-1, -2, and -3 have been synthesiz...
As a build-up to the synthesis of the proposed structure of azaspiracid, both enantiomers of fragmen...
Syntheses of the three key building blocks (65, 98, and 100) required for the total synthesis of the...
Syntheses of the three key building blocks (65, 98, and 100) required for the total synthesis of the...
A highly stereoselective and convergent approach for the key intermediate of the FGHI ring system of...
A convergent and stereoselective total synthesis of the previously assigned structure of azaspiracid...
The 39 steps: The recently proposed revised structures of azaspiracid-2 and -3 (see picture), the tw...
An illusive target: The two proposed structures of azaspiracid-1 (1 and FGHI-epi-1), were synthesize...
Graduation date: 2013Azaspiracid-1, a novel marine toxin that contains 9 rings and 20 stereogenic ce...
A convergent and stereoselective total synthesis of the previously assigned structure of azaspiracid...
The key building blocks (6, 7, and 8) for the intended construction of the originally proposed struc...
Access restricted to the OSU CommunityDiscussed herein is the evolution of the strategies for the sy...
A stereoselective synthesis of the ABCD ring framework of azaspiracid-1 and azaspiracid-3 has been a...
The previously accepted structure of the marine toxin azaspiracid\u20103 is revised based upon an or...
An efficient synthesis of the C1–C21 fragment of azaspiracids-1 and −3 is described. This features a...
The naturally occurring but scarce marine neurotoxins azaspiracids-1, -2, and -3 have been synthesiz...