185810-83-7

Upstream product

• 100-39-0 benzyl bromide 
• 665-27-0 1,5-quinide 
• 77-95-2 D-(-)-quinic acid 

Downstream Products

• 185810-84-8 (1S,3R,4R,5R)-3-Benzyloxy-1,4-dimethoxy-6-oxa-bicyclo[3.2.1]octan-7-one 
• 543724-49-8 (1S,3R,4R,5R)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-1-hydroxy-6-oxa-bicyclo[3.2.1]octan-7-one 
• 862791-08-0 (1S,3R,4R,5R)-3-benzyloxy-1,4-bis(tert-butyldimethylsilyloxy)cyclohexane-1,5-carbolactone 
• 862791-64-8 (1R,3R,4R)-1,4-dihydroxy-5-phenylcyclohex-5-ene-1,3-carbolactone 
• 862791-67-1 (1R,3R,4R)-1,4-dihydroxy-5-(4-fluorophenyl)cyclohex-5-ene-1,3-carbolactone 
• 862791-73-9 (1R,3R,4R)-1,4-dihydroxy-5-(3-fluorophenyl)cyclohex-5-ene-1,3-carbolactone 
• 862791-77-3 (1R,3R,4R)-1,4-dihydroxy-5-(3-hydroxyphenyl)cyclohex-5-ene-1,3-carbolactone 
• 862791-79-5 (1R,3R,4R)-1,4-dihydroxy-5-(3-nitrophenyl)cyclohex-5-ene-1,3-carbolactone 
• 862791-83-1 (1R,3R,4R)-1,4-dihydroxy-5-(3,5-difluorophenyl)cyclohex-5-ene-1,3-carbolactone 
• 862791-81-9 3-((1R,4R,5R)-1,4-Dihydroxy-7-oxo-6-oxa-bicyclo[3.2.1]oct-2-en-3-yl)-benzoic acid methyl ester 
• 862791-75-1 (1R,3R,4R)-1,4-dihydroxy-5-[3-(trifluoromethyl)phenyl]cyclohex-5-ene-1,3-carbolactone 
• 862791-71-7 (1R,3R,4R)-1,4-dihydroxy-5-[4-(trifluoromethyl)phenyl]cyclohex-5-ene-1,3-carbolactone 

Relevant academic research and scientific papers

Design and synthesis of mimics of S-Adenosyl-L-homocysteine as potential inhibitors of erythromycin methyltransferases

A series of indanotriazine C-ribosides were prepared as SAH mimics, and tested for their ability to inhibit erythromycin resistance methylases Erm AM and Erm C'. A carbocyclic analogue derived from quinic acid was also synthesized and tested. (C) 2000 Elsevier Science Ltd. All rights reserved.

Total synthesis of (-)-reserpine using the chiron approach

A highly stereocontrolled synthesis of ring D/E precursor to reserpine has been developed starting from (-)-quinic acid as a chiral template. The total synthesis of (-)-reserpine is described through the cyclization of an immonium lactam intermediate.