The origin of a common compound about 415918-91-1

There is still a lot of research devoted to this compound(SMILES:C[C@@H](N(P1OC2=CC=C3C=CC=CC3=C2C4=C5C=CC=CC5=CC=C4O1)[C@@H](C6=CC=CC=C6)C)C7=CC=CC=C7)Synthetic Route of C36H30NO2P, and with the development of science, more effects of this compound(415918-91-1) can be discovered.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 415918-91-1, is researched, SMILESS is C[C@@H](N(P1OC2=CC=C3C=CC=CC3=C2C4=C5C=CC=CC5=CC=C4O1)[C@@H](C6=CC=CC=C6)C)C7=CC=CC=C7, Molecular C36H30NO2PJournal, Article, Organic & Biomolecular Chemistry called Application of iridium catalyzed allylic substitution reactions in the synthesis of branched tryptamines and homologues via tandem hydroformylation-Fischer indole synthesis, Author is Bondzic, Bojan P.; Farwick, Andreas; Liebich, Jens; Eilbracht, Peter, the main research direction is tryptamine preparation allylic substitution iridium catalyst; hydroformylation Fischer indole synthesis iridium allylic substitution.Synthetic Route of C36H30NO2P.

Combination of enantioselective allylation reactions with a tandem hydroformylation-Fischer indole synthesis sequence as a highly diversity-oriented strategy for the synthesis of tryptamines and homologues was explored. This modular approach allows the substituents at C3 of the indole core, the type of the amine moiety, and the distance of the amine moiety to the indole core in the final synthetic step to be defined. The starting materials required for the hydroformylation step were synthesized via iridium catalyzed enantioselective allylic substitution reactions in high yields and excellent enantioselectivities. The Rh catalyzed hydroformylation step in the presence of Ph hydrazine, allows the in situ formed aldehyde to be trapped as the hydrazone. Subsequent acid catalyzed indolization furnishes the desired indole structures, e.g. I, in moderate to good yields.

There is still a lot of research devoted to this compound(SMILES:C[C@@H](N(P1OC2=CC=C3C=CC=CC3=C2C4=C5C=CC=CC5=CC=C4O1)[C@@H](C6=CC=CC=C6)C)C7=CC=CC=C7)Synthetic Route of C36H30NO2P, and with the development of science, more effects of this compound(415918-91-1) can be discovered.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics