Substituted alkenediols by alkylative double ring opening of dihydrofuran and dihydropyran epoxides.
[reaction: see text]. Dihydrofuran and dihydropyran epoxides undergo alkylative double ring opening with organolithiums to provide a new route to substituted alkenediols.
Main Authors: | Hodgson, D, Stent, M, Wilson, F |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2001
|
Similar Items
-
Organolithium-induced synthesis of unsaturated diols from epoxides of dihydrofurans and dihydropyrans
by: Hodgson, D, et al.
Published: (2002) -
Enantioselective alkylative double ring-opening of epoxides derived from cyclic allylic ethers: synthesis of enantioenriched unsaturated diols.
by: Hodgson, D, et al.
Published: (2003) -
Enantioselective alkylative double ring opening of epoxides: synthesis of enantioenriched unsaturated diols and amino alcohols.
by: Hodgson, D, et al.
Published: (2002) -
Organolithium-induced enantioselective alkylative double ring-opening of epoxides: synthesis of enantioenriched unsaturated amino alcohols
by: Hodgson, D, et al.
Published: (2004) -
Stereochemistry of Chiral 2-Substituted Chromanes: Twist of the Dihydropyran Ring and Specific Optical Rotation
by: Bei-Bei Yang, et al.
Published: (2023-01-01)