The first stereoselective total synthesis of neosemburin and isoneosemburin

2014 ◽  
Vol 12 (42) ◽  
pp. 8408-8414 ◽  
Author(s):  
Gadi Madhusudhan Reddy ◽  
Perali Ramu Sridhar
Keyword(s):  
Total Synthesis ◽  
Claisen Rearrangement ◽  
Vinyl Ethers ◽  
Allyl Vinyl Ethers

The stereoselective total synthesis of neosemburin and isoneosemburin was achieved using 3-C-branched sugar precursors which in turn were synthesized by Claisen rearrangement of sugar derived allyl vinyl ethers.

ChemInform Abstract: Catalytic Asymmetric Claisen Rearrangement of Gosteli-Type Allyl Vinyl Ethers: Total Synthesis of (-)-9,10-Dihydroecklonialactone B.

ChemInform ◽  
2014 ◽  
Vol 45 (39) ◽  
pp. no-no
Author(s):  
Julia Becker ◽  
Lena Butt ◽  
Valeska von Kiedrowski ◽  
Elisabeth Mischler ◽  
Florian Quentin ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Claisen Rearrangement ◽  
Vinyl Ethers ◽  
Catalytic Asymmetric ◽  
Allyl Vinyl Ethers

Catalytic Asymmetric Claisen Rearrangement of Gosteli-Type Allyl Vinyl Ethers: Total Synthesis of (−)-9,10-Dihydroecklonialactone B

2014 ◽  
Vol 79 (7) ◽  
pp. 3040-3051 ◽  
Author(s):  
Julia Becker ◽  
Lena Butt ◽  
Valeska von Kiedrowski ◽  
Elisabeth Mischler ◽  
Florian Quentin ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Claisen Rearrangement ◽  
Vinyl Ethers ◽  
Catalytic Asymmetric ◽  
Allyl Vinyl Ethers

Stereochemical aspects of the Claisen rearrangement of allyl vinyl ethers

1975 ◽  
Vol 40 (1) ◽  
pp. 86-92 ◽  
Author(s):  
Herbert O. House ◽  
Jacek Lubinkowski ◽  
James J. Good
Keyword(s):  
Claisen Rearrangement ◽  
Vinyl Ethers ◽  
Allyl Vinyl Ethers
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