Stereoselective additions to the cyclobutene double bond via homoconjugation.

Date

1977

Author

Tanlak, Melek

Metadata

Show full item record

Item Usage Stats

82
views

0
downloads

URI

https://hdl.handle.net/11511/8023

Collections

Graduate School of Natural and Applied Sciences, Thesis

Suggestions

OpenMETU
Core

Stereoselective additions to the norbornene double bond via bishomoconjugation. Bozoğlu, Faruk; Department of Chemistry (1977)
Stereoselective nucleophilic addition to the norborne double bond via bishomocon jugaton Gayretli, Zeki; Sayraç, Tuğmac; Department of Chemistry (1991)
Stereoselective nucleophilic addition to the olefinic double bond of endo-2-phenacly-5-norbornene via trishomoconjugation Doğan, Özdemir; Sayraç, Tuğmac; Department of Chemistry (1991)
Stereoselective oxidation of sulfides to sulfoxides by n-chloramines İpek, Halil; Akdağ, Akın; Department of Chemistry (2014) Chiral sulfoxides are present in many biologically active compounds. Asymmetric synthesis of the sulfoxides has been performed by chiral metal complexes and chiral peroxides. Although the asymmetric organooxidation of sulfides by chiral peroxides proved to be successful, peroxides are difficult to handle and obtain. In this study, a new metal free method has been developed to oxidize sulfides to chiral sulfoxides with easily accessible chiral N-chloramines. For this purpose, chiral reagents were synthesized...
Stereoselective synthesis of optically active dihydrofurans and dihydropyrans via a ring closing metathesis reaction ÇAYİR, Merve; Demirci, Sema; Sezer, Serdar; Tanyeli, Cihangir (Elsevier BV, 2011-06-15) A ring closing metathesis reaction of dienes and a ring closing enyne metathesis reaction derived from allyl, homoallyl and homopropargyl alcohol backbones are described. 2-Heteroaryl substituted allyl, homoallyl and homopropargyl alcohols have been easily and efficiently resolved through enzymatic resolution with high ee (93-99%) and known stereochemistry. Enantiomerically enriched dienes derived from allyl and homoallyl alcohols afforded the corresponding enantiomerically enriched dihydrofuran and dihydro...

Citation Formats

M. Tanlak, “Stereoselective additions to the cyclobutene double bond via homoconjugation.,” Middle East Technical University, 1977.