The use of butane diacetals of glycolic acid as precursors for the synthesis of the phytotoxic calmodulin inhibitor herbarumin II
The total synthesis of phytotoxic nonenolide herbarumin II (1) has been achieved by implementation of butane diacetal (BDA)-desymmetrised glycolate building blocks. Three of the four stereogenic centres present in the key coupling fragments were generated from both enantiomeric forms of the BDA buil...
Հիմնական հեղինակներ: | Diez, E, Dixon, D, Ley, S, Polara, A, Rodriguez, F |
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Ձևաչափ: | Journal article |
Լեզու: | English |
Հրապարակվել է: |
2003
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Նմանատիպ նյութեր
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Total synthesis of the phytotoxic agent herbarumin II using butane diacetals of glycolic acid as building blocks
: Diez, E, և այլն
Հրապարակվել է: (2003) -
Highly diastereoselective ketone aldol reactions of butane-2,3-diacetal desymmetrised glycolic acid
: Dixon, D, և այլն
Հրապարակվել է: (2002) -
Highly diastereoselective lithium enolate aldol reactions of butane-2,3-diacetal desymmetrized glycolic acid and deprotection to enantiopure anti-2,3-dihydroxy esters.
: Dixon, D, և այլն
Հրապարակվել է: (2001) -
Butane-2,3-diacetal-desymmetrized glycolic acid—a new building block for the stereoselective synthesis of enantiopure α-hydroxy acids
: Díez, E, և այլն
Հրապարակվել է: (2001) -
Studies on the generation of enolate anions from butane-2,3-diacetal protected glycolic acid derivatives and subsequent highly diastereoselective coupling reactions with aldehydes and acid chlorides
: Ley, S, և այլն
Հրապարակվել է: (2004)