Phenylsulfinylselenyl chloride (PhSO2SeCl): a new reagent for the formation of C–Se and N–Se bonds. Generation and in situ Diels–Alder trapping of selenonitrosoarene intermediates (Ar

Phenylsulfinylselenyl chloride (PhSO2SeCl): a new reagent for the formation of C–Se and N–Se bonds. Generation and in situ Diels–Alder trapping of selenonitrosoarene intermediates (Ar–NSe)

Published:1995 Issue:2 Volume: Page:195-196
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Bryce Martin R.,Chesney Antony

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1995/C3/C39950000195

Reference20 articles.

1. Organic sulfur chemistry. 26. Synthesis and reactions of some new sulfur transfer reagents

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3. Use of piperidine-1-sulphenyl chloride as a sulphur-transfer reagent in reactions with diamines: the preparation of sulphur–nitrogen heterocycles

4. Generation of thionitrosoarenes (ArNS) from N-(arylaminothio)phthalimides and in situ trapping with alkenes and conjugated dienes

5. Diels–Alder and ene reactions of new transient thionitrosoarenes (Ar-NS) and thionitrosoheteroarenes (Het–NS) generated from N-(arylaminosulfanyl)and N-(heteroarylaminosulfanyl)-phthalimides: synthesis of cyclic and acyclic sulfenamides

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