Concerning the 1,5-stereocontrol in tin(iv) chloride promoted reactions of 4- and 5-alkoxyalk-2-enylstannanes: trapping intermediate allyltin trichlorides using phenyllithium-Reference-Cited by-同舟云学术

Concerning the 1,5-stereocontrol in tin(iv) chloride promoted reactions of 4- and 5-alkoxyalk-2-enylstannanes: trapping intermediate allyltin trichlorides using phenyllithium

Published:2012 Issue:37 Volume:10 Page:7510
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Hobson Lindsay A.,Thomas Eric J.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2012/OB/C2OB25765C

Reference25 articles.

1. Remote stereocontrol using functionalized allylmetal reagents

2. Control and applications of remote asymmetric induction using allylmetal reagents

3. Effective 1,5-, 1,6- and 1,7-remote stereocontrol in reactions of alkoxy- and hydroxy-substituted allylstannanes with aldehydes

4. Effective 1,5-Asymmetric Induction in Tin(IV) Chloride Promoted Reactions Between Aldehydes and (4-Alkoxy-2-alkenyl)tributylstannanes

5. 1,5-Stereocontrol in tin(IV) halide mediated reactions between N- and S-substituted pent-2-enylstannanes and aldehydes or imines

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