Pd(II)-Catalyzed Enantioselective Ring-Contraction for the Construction of 1,4-Benzoxazines

Thermal Ring Contraction of a 1,4-Diazepine. Part II

ChemSpider Synthetic Pages ◽

10.1039/sp576 ◽

2012 ◽

Author(s):

Ramesha Ramakrishna

Keyword(s):

Ring Contraction

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Thermal Ring Contraction of a 1,4-Diazepine

ChemSpider Synthetic Pages ◽

10.1039/sp574 ◽

2012 ◽

Author(s):

Ramesha Ramakrishna

Keyword(s):

Ring Contraction

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ChemInform Abstract: LIGHT-INDUCED REACTION OF BORACYCLANES WITH BROMINE IN THE PRESENCE OF WATER, RING CONTRACTION OF BORACYCLANES TO PRODUCE CARBOCYCLIC STRUCTURES

Chemischer Informationsdienst ◽

10.1002/chin.197405235 ◽

1974 ◽

Vol 5 (5) ◽

pp. no-no

Author(s):

Y. YAMAMOTO ◽

H. C. BROWN

Keyword(s):

Ring Contraction ◽

Water Ring ◽

Induced Reaction

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The Influence of Anomeric Configuration and Aglycone Structure on the Outcome of Acid‐Promoted Ring Contraction in 2,3‐Di‐ O ‐Silylated S‐Galactopyranosides

ChemistrySelect ◽

10.1002/slct.202101441 ◽

2021 ◽

Vol 6 (24) ◽

pp. 6223-6229

Author(s):

Polina I. Abronina ◽

Alexander I. Zinin ◽

Nelly N. Malysheva ◽

Maxim Y. Karpenko ◽

Natalya G. Kolotyrkina ◽

...

Keyword(s):

Ring Contraction ◽

Anomeric Configuration

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N-Chlorinative Ring Contraction of 1,4-Dimethoxyphthalazines via a Bicyclization/Ring-Opening Mechanism

Synthesis ◽

10.1055/s-0040-1706639 ◽

2020 ◽

Author(s):

Jeong Kyun Im ◽

Ilju Jeong ◽

Jun-Ho Choi ◽

Won-jin Chung ◽

ByeongDo Yang ◽

...

Keyword(s):

Ring Opening ◽

Reaction Conditions ◽

Ring Contraction ◽

Silyl Group ◽

Favorskii Rearrangement ◽

Mechanistic Analysis ◽

Group A ◽

Overall Efficiency ◽

Trichloroisocyanuric Acid

AbstractAn unprecedented N-chlorinative ring contraction of 1,2-diazines was discovered and investigated with an electrophilic chlorinating reagent, trichloroisocyanuric acid (TCICA). Through optimization and mechanistic analysis, the assisting role of n-Bu4NCl as an exogenous nucleophile was identified, and the optimized reaction conditions were applied to a range of 1,4-dimethoxyphthalazine derivatives. Also, an improvement of overall efficiency was demonstrated by the use of a labile O-silyl group. A bicyclization/ring-opening mechanism, inspired by the Favorskii rearrangement, was proposed and supported by the DFT calculations. Furthermore, the efforts on scope expansion as well as the evaluation of other electrophilic promoters revealed that the newly developed ring contraction reactivity is a unique characteristic of 1,4-dimethoxyphthalazine scaffold and TCICA.

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