المؤلفون: Ksenia Malkova, Ilya Tatarinov, Grigory Kantin, Dmitry Dar’in

مصطلحات موضوعية: Biochemistry, Medicine, Microbiology, Genetics, Pharmacology, Biotechnology, Ecology, Inorganic Chemistry, Infectious Diseases, Virology, Computational Biology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, – h insertion, utilizing allenic acids, ii )- catalyzed, allenic acids followed, polysubstituted spirocyclic butenolides, heterocyclic diazo compounds, diverse spirocyclic scaffolds, diazo tetramic acids, furanones via rh, spirocyclic δ, spirocyclic 2, diazo oxindoles, diazo homophthalimides, two types, research revealed, promoted cyclization

Relation: https://figshare.com/articles/journal_contribution/Utilizing_Allenic_Acids_and_Heterocyclic_Diazo_Compounds_in_the_Synthesis_of_Polysubstituted_Spirocyclic_Butenolides_and_Methylidene_2_Furanones/25125435

الاتاحة: https://doi.org/10.1021/acs.joc.3c02474.s001
https://figshare.com/articles/journal_contribution/Utilizing_Allenic_Acids_and_Heterocyclic_Diazo_Compounds_in_the_Synthesis_of_Polysubstituted_Spirocyclic_Butenolides_and_Methylidene_2_Furanones/25125435

المؤلفون: Ksenia Malkova, Ilya Tatarinov, Grigory Kantin, Dmitry Dar’in

مصطلحات موضوعية: Biochemistry, Medicine, Microbiology, Genetics, Pharmacology, Biotechnology, Ecology, Inorganic Chemistry, Infectious Diseases, Virology, Computational Biology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, – h insertion, utilizing allenic acids, ii )- catalyzed, allenic acids followed, polysubstituted spirocyclic butenolides, heterocyclic diazo compounds, diverse spirocyclic scaffolds, diazo tetramic acids, furanones via rh, spirocyclic δ, spirocyclic 2, diazo oxindoles, diazo homophthalimides, two types, research revealed, promoted cyclization

Relation: https://figshare.com/articles/journal_contribution/Utilizing_Allenic_Acids_and_Heterocyclic_Diazo_Compounds_in_the_Synthesis_of_Polysubstituted_Spirocyclic_Butenolides_and_Methylidene_2_Furanones/25125435

الاتاحة: https://doi.org/10.1021/acs.joc.3c02474.s001

المؤلفون: Dmitry Dar’in (1555282), Grigory Kantin (6448364), Daria Glushakova (14334845), Vladimir Sharoyko (8535474), Mikhail Krasavin (820851)

مصطلحات موضوعية: Biochemistry, Medicine, Genetics, Pharmacology, Ecology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, – h insertion, thereby demonstrating quite, ii )- catalyzed, diazocarbonyl compounds suitable, propiolic acids though, propiolic acids followed, generally high yields, promoted cyclization 3, like spirocyclic δ, diazotetramic acids, like δ, high diastereoselectivity, virtually insensitive, valid substrates, target δ, somewhat sensitive, new class, monosubstituted 3, large scope, chiral 5, approach outlined

Relation: https://figshare.com/articles/journal_contribution/Diazo_Tetramic_Acids_Provide_Access_to_Natural-Like_Spirocyclic_sup_sup_-Butenolides_through_Rh_II_-Catalyzed_O_H_Insertion_Base-Promoted_Cyclization/21824771

الاتاحة: https://doi.org/10.1021/acs.joc.2c02600.s001

المؤلفون: Dmitry Dar’in, Grigory Kantin, Daria Glushakova, Vladimir Sharoyko, Mikhail Krasavin

مصطلحات موضوعية: Biochemistry, Medicine, Genetics, Pharmacology, Ecology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, – h insertion, thereby demonstrating quite, ii )- catalyzed, diazocarbonyl compounds suitable, propiolic acids though, propiolic acids followed, generally high yields, promoted cyclization 3, like spirocyclic δ, diazotetramic acids, like δ, high diastereoselectivity, virtually insensitive, valid substrates, target δ, somewhat sensitive, new class, monosubstituted 3, large scope, chiral 5, approach outlined

Relation: https://doi.org/10.1021/acs.joc.2c02600.s001

الاتاحة: https://doi.org/10.1021/acs.joc.2c02600.s001