reference/3393323

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3393323

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	2982
issn	1523-7052 1523-7060
issueIdentifier	16
pageRange	2978-2982
publicationName	Organic Letters
startingPage	2978
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_c7576a8b74cd0901db3fcc44ee2fad6f http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_487baf6554eb36bb22c6138d90a7c50f http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_a71960533e57bbfecb38e66869a95032 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_d813a34c1e4381504d2b075a53f74917
bibliographicCitation	Xu S, Huang A, Yang Y, Wang Y, Zhang M, Sun Z, Zhao M, Wei Y, Li G, Hong L. Organocatalytic Enantioselective Construction of Spiroketal Lactones Bearing Axial and Central Chirality via an Asymmetric Domino Reaction. Org Lett. 2022 Apr 29;24(16):2978–82. doi: 10.1021/acs.orglett.2c00845. PMID: 35380447.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_4f995265ebb6ad5583c07cdae93efced http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_99a4644d79c27f99b5518d402fb5d861 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_860754db7cc49d75b33fee5f2875440b http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_080011f67ff84be10359fbd737e3a48d http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-3489-0633 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0558341d18f07eadf3cb5ce228ed2747 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_645bd5c7c983695f685c121707d165d3 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-7528-2036 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_cc8a2d82e9c2cd3c8f24f651bd413452 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7f2fffcfe6204568b9e657d867993e37
date	2022-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1021/acs.orglett.2c00845 https://pubmed.ncbi.nlm.nih.gov/35380447
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Organocatalytic Enantioselective Construction of Spiroketal Lactones Bearing Axial and Central Chirality via an Asymmetric Domino Reaction
discusses	http://id.nlm.nih.gov/mesh/M0008898 http://id.nlm.nih.gov/mesh/M0020345 http://id.nlm.nih.gov/mesh/M0012175 http://id.nlm.nih.gov/mesh/M0511023
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hasSubjectTerm	http://id.nlm.nih.gov/mesh/D013237 http://id.nlm.nih.gov/mesh/D005663

Total number of triples: 41.