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A Modular Approach to Angularly Fused Polyquinanes via Ring..:
Sambasivarao Kotha (1528336)
;
Ramakrishna Reddy Keesari (8156418)
https://figshare.com/articles/journal_contribution/A_Modular_Approach_to_Angularly_Fused_Polyquinanes_via_Ring-Rearrangement_Metathesis_Synthetic_Access_to_Cameroonanol_Analogues_and_the_Basic_Core_of_Subergorgic_Acid_and_Crinipellin/17033373. , 2021
Link:
https://doi.org/10.1021/acs.joc.1c02258.s001
RT Journal T1
A Modular Approach to Angularly Fused Polyquinanes via Ring-Rearrangement Metathesis: Synthetic Access to Cameroonanol Analogues and the Basic Core of Subergorgic Acid and Crinipellin
UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_17033373&Exemplar=1&LAN=DE A1 Sambasivarao Kotha (1528336) A1 Ramakrishna Reddy Keesari (8156418) YR 2021 K1 Biophysics K1 Biochemistry K1 Genetics K1 Neuroscience K1 Pharmacology K1 Biotechnology K1 Ecology K1 Chemical Sciences not elsewhere classified K1 ray diffraction studies K1 newly reported tri K1 many natural products K1 angularly fused polyquinanes K1 one (< b K1 7 </ b K1 6 </ b K1 subergorgic acid core K1 present strategy relies K1 subergorgic acid K1 exo </ K1 core units K1 basic core K1 worth mentioning K1 work highlights K1 tetraquinane skeletons K1 synthetic access K1 stereoselective ring K1 stereoselective reduction K1 relative stereochemistry K1 rearrangement metathesis K1 nmr data K1 new molecules K1 modular approach K1 medicinal chemistry K1 mediated coupling K1 less explored K1 key step K1 key reactions K1 junction allylation K1 excellent yields K1 ester derivatives K1 employing atom K1 economic ring K1 crystal x K1 critical step K1 chemical space K1 chemical methods K1 carbonyl group K1 >- dicyclopentadiene JF https://figshare.com/articles/journal_contribution/A_Modular_Approach_to_Angularly_Fused_Polyquinanes_via_Ring-Rearrangement_Metathesis_Synthetic_Access_to_Cameroonanol_Analogues_and_the_Basic_Core_of_Subergorgic_Acid_and_Crinipellin/17033373 LK http://dx.doi.org/https://doi.org/10.1021/acs.joc.1c02258.s001 DO https://doi.org/10.1021/acs.joc.1c02258.s001 SF ELIB - SuUB Bremen
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