Eissler S, Neumann B, Stammler H-G, Sewald N. Synthetic routes towards cryptophycin unit A diastereomers. SYNLETT. 2008;2008(2):273-277.Unit A of cryptophycin 1 is a delta-hydroxy acid with four stereogenic centres. Our unit A synthesis introduces the first two stereogenic centres by a catalytic, asymmetric dihydroxylation, whereas the remaining two stereogenic centres are established by diastereoselective reactions. In this letter, we focus on the diastereoselectivity of these reactions and discuss the accessibility of cryptophycin unit A diastereomers
The cryptophycins are a family of macrocyclic depsipeptide natural products that display exceptional...
Weiss C, Sammet B, Sewald N. Recent approaches for the synthesis of modified cryptophycins. Natural ...
threo-\u3b1-Dibenzylamino-beta-hydroxyesters (2) have been synthesised with high diastereoselectivit...
Mast CA, Eissler S, Stoncius A, Stammler H-G, Neumann B, Sewald N. Efficient and versatile stereosel...
Sammet B, Brax M, Sewald N. A two step synthesis of a key unit B precursor of cryptophycins by asymm...
Sammet B, Radzey H, Neumann B, Stammler H-G, Sewald N. Cryptophycin-39 Unit A Precursor Synthesis by...
Indian Institute of Chemical Technology, Hyderabad-500 007, India Manuscript received 6 September 1...
Eissler S, Stoncius A, Nahrwold M, Sewald N. The synthesis of cryptophycins. SYNTHESIS. 2006;2006(22...
A stereoselective total synthesis of (+)-cryptocarya diacetate (1) was achieved by two different rou...
Sammet B, Bogner T, Nahrwold M, Weiss C, Sewald N. Approaches for the Synthesis of Functionalized Cr...
[reaction: see text] Herein, we report a diastereoselective synthesis of the natural product (2S,5R)...
Eißler S. Synthese von Cryptophycinen für SAR-Studien. Bielefeld (Germany): Bielefeld University; 20...
The first total synthesis of cryptopyranmoscatone A1 isolated from Cryptocarya moschata has been acc...
A highly stereoselective synthesis of (+)-cryptocarya diacetate is achieved through our recently dev...
The total synthesis and structural revision of (+)-cryptoconcatone H are described. Guided by comput...
The cryptophycins are a family of macrocyclic depsipeptide natural products that display exceptional...
Weiss C, Sammet B, Sewald N. Recent approaches for the synthesis of modified cryptophycins. Natural ...
threo-\u3b1-Dibenzylamino-beta-hydroxyesters (2) have been synthesised with high diastereoselectivit...
Mast CA, Eissler S, Stoncius A, Stammler H-G, Neumann B, Sewald N. Efficient and versatile stereosel...
Sammet B, Brax M, Sewald N. A two step synthesis of a key unit B precursor of cryptophycins by asymm...
Sammet B, Radzey H, Neumann B, Stammler H-G, Sewald N. Cryptophycin-39 Unit A Precursor Synthesis by...
Indian Institute of Chemical Technology, Hyderabad-500 007, India Manuscript received 6 September 1...
Eissler S, Stoncius A, Nahrwold M, Sewald N. The synthesis of cryptophycins. SYNTHESIS. 2006;2006(22...
A stereoselective total synthesis of (+)-cryptocarya diacetate (1) was achieved by two different rou...
Sammet B, Bogner T, Nahrwold M, Weiss C, Sewald N. Approaches for the Synthesis of Functionalized Cr...
[reaction: see text] Herein, we report a diastereoselective synthesis of the natural product (2S,5R)...
Eißler S. Synthese von Cryptophycinen für SAR-Studien. Bielefeld (Germany): Bielefeld University; 20...
The first total synthesis of cryptopyranmoscatone A1 isolated from Cryptocarya moschata has been acc...
A highly stereoselective synthesis of (+)-cryptocarya diacetate is achieved through our recently dev...
The total synthesis and structural revision of (+)-cryptoconcatone H are described. Guided by comput...
The cryptophycins are a family of macrocyclic depsipeptide natural products that display exceptional...
Weiss C, Sammet B, Sewald N. Recent approaches for the synthesis of modified cryptophycins. Natural ...
threo-\u3b1-Dibenzylamino-beta-hydroxyesters (2) have been synthesised with high diastereoselectivit...