196503-55-6

Upstream product

• 41995-26-0 benzyl isocyanoacetate 
• 196503-54-5 (1S,2S,3R,4R)-5-Benzenesulfonyl-3-carbamoyl-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid methyl ester 
• 186581-53-3 diazomethane 
• 196503-53-4 (-)-(1R,2R,3R,6S,7S,9R)-5-oxo-2-exo-(phenylsulfonyl)-4-oxatricyclo[4.2.1.0^3,7]nonane-9-exo-carboxamide 
• 70190-87-3 (1R,2S,3S,4S)-bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid 
• 196503-51-2 (1R,2R,3R,6S,7S,9R)-5-Oxo-2-phenylsulfanyl-4-oxa-tricyclo[4.2.1.0^3,7]nonane-9-carboxylic acid 
• 196503-52-3 (1R,2R,3R,6S,7S,9R)-5-Oxo-2-phenylsulfanyl-4-oxa-tricyclo[4.2.1.0^3,7]nonane-9-carboxylic acid amide 

Downstream Products

• 952117-59-8 1-benzyl-6-methyl-[(4R,5S,6S,7S)-5-cyano-3-formyl-4,5,6,7-tetrahydro-4,7-methano-2H-isoindole-1,6-dicarboxylate] 

Relevant academic research and scientific papers

Synthesis of a peptide-linked chlorin dyad as a model compound for the photosynthetic reaction centre

The enantiomerically pure chlorins 19 and 21 were synthesised from tripyrrolic nickel complex rac-17 and pyrrole building blocks 12 and 16. The pyrroles are annelated with norbornane moieties which contain the chiral information as well as two different f

A simple and flexible synthesis of pyrroles from α,β-unsaturated sulfones

The addition of alkyl isocyanoacetates and isocyanoacetonitrile to α,β-unsaturated sulfones affords a convenient and broad access to pyrroles with unusual substitution patterns (see Scheme 2). The α,β-unsaturated sulfones required as starting materials ar

Synthesis of a Novel Enantiomerically Pure Chlorin as a Potential Subunit for an Artificial Photosynthetic Reaction Center

The total synthesis of an enantiomerically pure chlorin with two different functional groups as a potential subunit for the construction of artificial photosynthetic reaction centers was achieved.