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An effective one-pot access to polynuclear dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties via a 1,3-dipolar cycloaddition strategy.


ABSTRACT: An effective and highly regio- and diastereoselective one-pot method for the synthesis of new polynuclear dispiroheterocyclic systems with five stereogenic centers (dispiro[imidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazine-6,3'-pyrrolidine-2',3''-indoles]) comprising pyrrolidinyloxindole and imidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazine moieties has been developed. The method relies on a 1,3-dipolar cycloaddition of azomethine ylides generated in situ from isatin derivatives and sarcosine to 6-benzylideneimidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazine-2,7-diones.

SUBMITTER: Izmest'ev AN 

PROVIDER: S-EPMC5238633 | biostudies-literature | 2016

REPOSITORIES: biostudies-literature

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An effective one-pot access to polynuclear dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties via a 1,3-dipolar cycloaddition strategy.

Izmest'ev Alexei N AN   Gazieva Galina A GA   Sigay Natalya V NV   Serkov Sergei A SA   Karnoukhova Valentina A VA   Kachala Vadim V VV   Shashkov Alexander S AS   Zanin Igor E IE   Kravchenko Angelina N AN   Makhova Nina N NN  

Beilstein journal of organic chemistry 20161024


An effective and highly regio- and diastereoselective one-pot method for the synthesis of new polynuclear dispiroheterocyclic systems with five stereogenic centers (dispiro[imidazo[4,5-<i>e</i>]thiazolo[3,2-<i>b</i>]-1,2,4-triazine-6,3'-pyrrolidine-2',3''-indoles]) comprising pyrrolidinyloxindole and imidazo[4,5-<i>e</i>]thiazolo[3,2-<i>b</i>]-1,2,4-triazine moieties has been developed. The method relies on a 1,3-dipolar cycloaddition of azomethine ylides generated in situ from isatin derivative  ...[more]

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