Alkyl radical cyclization to vinylogous carbonates for the stereoselective synthesis of unsymmetrical dioxa-cage compounds: Effect of conformation on the rate of cyclization versus reduction

Tetrahedron

Volumn 67, Issue 6, 2011, Pages 1216-1230

  Gharpure, Santosh J ^a   Porwal, Suheel K ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY MADRAS   (India)

Author keywords

Diels Alder reaction; Oxa cages; Oxymercuration; Radical cyclization; Vinylogous carbonates

Indexed keywords

ALCOHOL; ALKYL GROUP; CARBONIC ACID DERIVATIVE; IODINE; VINYL DERIVATIVE;

ARTICLE; ASYMMETRIC SYNTHESIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; DIELS ALDER REACTION; ETHERIFICATION; PRIORITY JOURNAL; REACTION ANALYSIS; REDUCTION; STEREOCHEMISTRY;

ALNUS;

EID: 78751581592     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.11.098     Document Type: Article

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76. 3; unit cell parameters: a=14.4267(16), b=6.2541(7), c=15.9204(17); space group: Pca2(1); CCDC number 652177. CCDC 652177 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via http://www.ccdc.cam.ac.uk/data-request/cif.
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81. 7; unit cell parameters: a=29.6325(10), b=5.9688(2), c=21.6208(8), β=121.391(3), space group: C(2)/c; CCDC number 652178.