<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Carrilho RM</submitter><funding>NHGRI NIH HHS</funding><pagination>o2370</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3200832</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>67(Pt 9)</volume><pubmed_abstract>The title compound, C(25)H(24)O(4), a meth-oxy-methyl (MOM) bis-protected BINOL derivative containing a methyl substituent in position 3, is a key inter-mediate for the synthesis of a great variety of chiral auxiliaries. The planes of the naphthyl aromatic rings are at an angle of 70.74 (3)°. There are no conventional hydrogen bonds binding the mol-ecules.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pubmed_title>2,2'-Bis(meth-oxy-meth-oxy)-3-methyl-1,1'-binaphth-yl.</pubmed_title><pmcid>PMC3200832</pmcid><funding_grant_id>R21 HG005065</funding_grant_id><pubmed_authors>Carrilho RM</pubmed_authors><pubmed_authors>Rodrigues VH</pubmed_authors><pubmed_authors>Abreu AR</pubmed_authors><pubmed_authors>Pereira MM</pubmed_authors></additional><is_claimable>false</is_claimable><name>2,2'-Bis(meth-oxy-meth-oxy)-3-methyl-1,1'-binaphth-yl.</name><description>The title compound, C(25)H(24)O(4), a meth-oxy-methyl (MOM) bis-protected BINOL derivative containing a methyl substituent in position 3, is a key inter-mediate for the synthesis of a great variety of chiral auxiliaries. The planes of the naphthyl aromatic rings are at an angle of 70.74 (3)°. There are no conventional hydrogen bonds binding the mol-ecules.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Sep</publication><modification>2025-04-04T08:06:19.95Z</modification><creation>2019-03-26T23:59:26Z</creation></dates><accession>S-EPMC3200832</accession><cross_references><pubmed>22058976</pubmed><doi>10.1107/S1600536811031722</doi></cross_references></HashMap>