115798-03-3

Upstream product

• 64312-89-6 Mosher's acid chloride 
• 115798-07-7 2,4,6-Triisopropyl-benzenesulfonic acid 2-hydroxy-2-(6-oxo-tetrahydro-pyran-2-yl)-ethyl ester 
• 6553-96-4 2,4,6-triisopropylphenylsulfonyl chloride 
• 115798-07-7 (5R,6S)-5,6-dihydroxy-7-(triisopropylbenzenesulfonyloxy)heptanoic-1,5-lactone 
• 115798-05-5 (5S,6R)-5,6-Dihydroxy-7-(2,4,6-triisopropyl-benzenesulfonyloxy)-heptanoic acid 
• 39637-99-5 (S)-(+)-2-methoxy-2-trifluoromethyl-2-phenylacetyl chloride 
• 129815-32-3 (5S,6R)-5,6-dihydroxy-7-(triisopropylbenzenesulfonyloxy)heptanoic-1,5-lactone 
• 115798-06-6 ethyl (5R,6S)-5,6-dihydroxy-7-(triisopropylbenzenesulfonyloxy)heptanoate 
• 79308-41-1 (5R,6S)-5,6,7-Trihydroxy-heptanoic acid ethyl ester 
• 115798-00-0 5,6-Dihydroxy-7-(2,4,6-triisopropyl-benzenesulfonyloxy)-heptanoic acid ethyl ester 
• 79308-41-1 5,6,7-Trihydroxy-heptanoic acid ethyl ester 

Relevant academic research and scientific papers

Inversion of configurations of contiguous carbinol centres: application to the synthesis of both enantiomers of natural products from the same enantiomerically pure starting material

A novel method for effecting the inversion of configuration of two and three contiguous carbinol centers in a diol, triol, and tetraol chain, thus affording the opposite enantiomer with >/=98percent e.e., has been developed.The method is based on the sequ

Inversion of Configurations of Contiguous Carbinol Centers

A simple method for effecting the inversion of configuration of two contiguous carbinol centers in a diol and triol chain, thus affording the opposite enantiomer, has been developed.Application of this methodology to the synthesis of an LTA4 in