Synthesis and Reactivity of Chiral Tellurium Azomethines: Pseudopolymorphism of [o-((((1S,2R)-2-Hydroxy-2-phenyl-1-methylethyl)amino)methinyl)phenyl]tellurium(IV) Bromide-Reference-Cited by-同舟云学术

Synthesis and Reactivity of Chiral Tellurium Azomethines: Pseudopolymorphism of [o-((((1S,2R)-2-Hydroxy-2-phenyl-1-methylethyl)amino)methinyl)phenyl]tellurium(IV) Bromide

Published:1997-02-01 Issue:4 Volume:16 Page:563-571
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Menon Saija C.¹,Singh Harkesh B.¹,Patel Rajan P.²,Das Kalyan³,Butcher Ray J.⁴

Affiliation:

1. Department of Chemistry, Indian Institute of Technology, Powai, Bombay 400 076, India

2. Chemistry Division, Bhabha Atomic Research Centre Trombay, Bombay 400 085, India

3. Molecular Biophysics Unit, Indian Institute of Science, Bangalore 560 012, India

4. Department of Chemistry, Howard University, Washington, D.C. 20059

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om9604280

Reference49 articles.

1. Asymmetric oxidation of simple selenides to selenoxides in high enantiopurity. Stereochemical aspects of the allyl selenoxide/allyl selenenate rearrangement

2. Asymmetric induction in the oxidation of [2.2]paracyclophane-substituted selenides. Application of chirality transfer in the selenoxide [2,3] sigmatropic rearrangement

3. Synthesis of [R,S;R,S]- and [S,R;S,R]-Bis[2-[1-(dimethylamino)ethyl]ferrocenyl] Diselenides and Their Application to Asymmetric Selenoxide Elimination and [2,3]Sigmatropic Rearrangement

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