The first total synthesis of cryptopyranmoscatone A1 isolated from Cryptocarya moschata has been accomplished from 3,4,6-tri-O-acetyl-D-glucal. In addition to the RCM and cross-metathesis (CM) reactions, the synthesis features a highly diastereoselective Brown's allylation reaction and sets the absolute stereochemistry of the natural product
A stereoselective total synthesis of (-)-cryptocaryol A (1) is described. Key features of the 17-ste...
This dissertation highlights the total synthesis of natural products that possess a C-glycoside moie...
The first asymmetric total synthesis of (1S,5R,7S)-cryptorigidifoliol G and (1S,5R,7R)-cryptorigidif...
The first stereoselective total synthesis of the natural cryptopyranmoscatone B1 has been accomplish...
Ring-closing metathesis (RCM) and olefin cross-metathesis (CM) reactions were used as the key steps ...
Cryptocaryol A is a stereochemically complex natural product with potential anticancer properties. ...
A highly stereoselective synthesis of (+)-cryptocarya diacetate is achieved through our recently dev...
A stereoselective total synthesis of (+)-cryptocarya diacetate (1) was achieved by two different rou...
Total syntheses of cryptofolione were accomplished by two different routes via a common intermediate...
A stereoselective total synthesis of (-)-cryptocaryol A () is described. Key features of the 17-step...
Eissler S, Neumann B, Stammler H-G, Sewald N. Synthetic routes towards cryptophycin unit A diastereo...
The total synthesis and structural revision of (+)-cryptoconcatone H are described. Guided by comput...
The total synthesis and structural revision of (+)-cryptoconcatone H are described. Guided by comput...
Polyhydroxylated fragments are ubiquitous in natural products possessing interesting biological prop...
Mast CA, Eissler S, Stoncius A, Stammler H-G, Neumann B, Sewald N. Efficient and versatile stereosel...
A stereoselective total synthesis of (-)-cryptocaryol A (1) is described. Key features of the 17-ste...
This dissertation highlights the total synthesis of natural products that possess a C-glycoside moie...
The first asymmetric total synthesis of (1S,5R,7S)-cryptorigidifoliol G and (1S,5R,7R)-cryptorigidif...
The first stereoselective total synthesis of the natural cryptopyranmoscatone B1 has been accomplish...
Ring-closing metathesis (RCM) and olefin cross-metathesis (CM) reactions were used as the key steps ...
Cryptocaryol A is a stereochemically complex natural product with potential anticancer properties. ...
A highly stereoselective synthesis of (+)-cryptocarya diacetate is achieved through our recently dev...
A stereoselective total synthesis of (+)-cryptocarya diacetate (1) was achieved by two different rou...
Total syntheses of cryptofolione were accomplished by two different routes via a common intermediate...
A stereoselective total synthesis of (-)-cryptocaryol A () is described. Key features of the 17-step...
Eissler S, Neumann B, Stammler H-G, Sewald N. Synthetic routes towards cryptophycin unit A diastereo...
The total synthesis and structural revision of (+)-cryptoconcatone H are described. Guided by comput...
The total synthesis and structural revision of (+)-cryptoconcatone H are described. Guided by comput...
Polyhydroxylated fragments are ubiquitous in natural products possessing interesting biological prop...
Mast CA, Eissler S, Stoncius A, Stammler H-G, Neumann B, Sewald N. Efficient and versatile stereosel...
A stereoselective total synthesis of (-)-cryptocaryol A (1) is described. Key features of the 17-ste...
This dissertation highlights the total synthesis of natural products that possess a C-glycoside moie...
The first asymmetric total synthesis of (1S,5R,7S)-cryptorigidifoliol G and (1S,5R,7R)-cryptorigidif...
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