Copper‐promoted Synthesis of β‐Selenylated Cyclopentanones via Selenylation and 1,2‐Alkyl Migration Sequences of Alkenyl Cyclobutanols

Copper‐promoted selenylation and semipinacol‐type rearrangement of alkenyl alcohols.

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Bibliographic Details
Published inBulletin of the Korean Chemical Society Vol. 41; no. 3; pp. 378 - 381
Main Authors Kim, Yubin, Kim, Dae Young
Format Journal Article
LanguageEnglish
Published Weinheim Wiley‐VCH Verlag GmbH & Co. KGaA 01.03.2020
Wiley
대한화학회
Subjects
Alkenyl cyclobutanols
Chemistry
Chemistry, Multidisciplinary
Diselenides
Physical Sciences
Science & Technology
Selenylation
Semipinacol‐type rearrangement
화학
N-PHENYL TETRAHYDROISOQUINOLINE
ASYMMETRIC-SYNTHESIS
RING EXPANSION
Selenylation
ORTHO-QUINONE METHIDES
ONE-POT SYNTHESIS
VISIBLE-LIGHT PHOTOREDOX
Diselenides
Alkenyl cyclobutanols
OXIDATIVE COUPLING REACTION
SEMIPINACOL REARRANGEMENT
KETO ACIDS
DECARBOXYLATIVE ALKYLATION
Semipinacol-type rearrangement
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Summary:Copper‐promoted selenylation and semipinacol‐type rearrangement of alkenyl alcohols.
Bibliography:https://onlinelibrary.wiley.com/doi/abs/10.1002/bkcs.11967
ISSN:1229-5949
0253-2964
1229-5949
DOI:10.1002/bkcs.11967