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Isoformononetin → (+)-Pisatin

HRID 2118272
Notes
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Reaction equation

HRID 2118272 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]2[C:9]([C:11]([C:14]3[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=3)=[CH:12][O:13][C:5]=2[CH:4]=1)=[O:10].[CH3:21][O:22]C1C=CC(C2C(=O)C3C=CC(O)=CC=3OC=2)=C(O)C=1.C[O:43]C1C=CC(C2C(=O)C3C=CC(O)=CC=3OC=2)=CC=1O.C1OC2C=C(C3C(=O)C4C=CC(O)=CC=4OC=3)C=CC=2O1>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]2[C@H:9]3[O:10][C:15]4[C:14](=[CH:19][C:18]5[O:22][CH2:21][O:20][C:17]=5[CH:16]=4)[C@@:11]3([OH:43])[CH2:12][O:13][C:5]=2[CH:4]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 3764IsoformononetinHCID 5280448CalycosinHCID 5280551Xenognosin BHCID 5281805Pseudobaptigenin

Product 1

HCID 101689(+)-Pisatin

Procedure

Isoformononetin, 2′-hydroxyformononetin, 3′-hydroxyformononetin (calycosin) and pseudobaptigenin were purchased from Apin (Abingdon, UK). Maackiairi and pisatin were kindly provided by Dr. H. D. VanEtten, (University of Arizona, Tucson). Maackiain glucoside and maackiain glucose malonate standards were gifts from Dr. S. Tebayashi (Kochi University, Japan). Medicarpin was from a lab collection. Other isoflavonoids were from Indofine Chemical Company (Somerville, N.J.). CO was obtained from Aldrich and all other chemicals were from Sigma (St. Louis, Mo.).

Sources & evidence

ORD record
ord-ed9baa25a6204d659367d335296acaf6
Source dataset
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07442851B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes