المؤلفون: Christopher Topp, Jan M. Metzler, Friedemann Dressler, Dominik Niedek, Sören M. M. Schuler, Peter R. Schreiner

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Biotechnology, Evolutionary Biology, Infectious Diseases, Computational Biology, Chemical Sciences not elsewhere classified, various ring sizes, spirovinylethylene carbonates broadens, pot cascade reaction, easy synthetic entry, spirocyclic vinylic carbonates, >- spirovinylethylene carbonates, spirocyclic scaffolds, spirocyclic scaffold, experiments approach, exo <, endo <, catalytic applications, allylic alcohols

Relation: https://figshare.com/articles/journal_contribution/Preparation_of_Spirocyclic_Vinylic_Carbonates_from_Allylic_Alcohols/24964303

الاتاحة: https://doi.org/10.1021/acs.orglett.3c03253.s001
https://figshare.com/articles/journal_contribution/Preparation_of_Spirocyclic_Vinylic_Carbonates_from_Allylic_Alcohols/24964303

المؤلفون: Xing He, Kangli Liu, Shengnan Yan, Yue Wang, Yuqin Jiang, Xinying Zhang, Xuesen Fan

مصطلحات موضوعية: Biochemistry, Genetics, Pharmacology, Ecology, Developmental Biology, Chemical Sciences not elsewhere classified, spiro element initiated, fused indolines tethered, find wide applications, diverse functional groups, unprecedented reaction pattern, mild reaction conditions, sophisticated spirocyclic skeleton, pharmaceutically valuable products, fused indoline skeleton, sustainable oxidant herein, sustainable oxidant, cascade reaction, spirocyclic scaffold, selected products, sustainable oxidants, title product, spiroindolinonyl moiety, spiroindolinone based, simultaneous introduction, related areas, reductive elimination, notable features, membered ru, lead compounds

Relation: https://figshare.com/articles/journal_contribution/Synthesis_of_1_7-Fused_Indolines_Tethered_with_Spiroindolinone_Based_on_C_H_Activation_Strategy_with_Air_as_a_Sustainable_Oxidant/25041715

الاتاحة: https://doi.org/10.1021/acs.joc.3c02630.s001
https://figshare.com/articles/journal_contribution/Synthesis_of_1_7-Fused_Indolines_Tethered_with_Spiroindolinone_Based_on_C_H_Activation_Strategy_with_Air_as_a_Sustainable_Oxidant/25041715

المؤلفون: Xingrong Liao (4400386), Fulin Zhou (1564051), Zhengyang Bin (1411951), Yudong Yang (185767), Jingsong You (1397368)

مصطلحات موضوعية: Biochemistry, Microbiology, Biotechnology, Ecology, Infectious Diseases, Space Science, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Annulation, spirocyclic scaffold, insertion, Palladium-Catalyzed Cascade Dearoma., quantum efficiency, aryl halides, spiroembedded polycyclic, cascade process, host material, approach, compound, Alkynes Described, Heck-type dearomatization, palladium-catalyzed, Aromatic Halides, sequential alkyne, optoelectronic study, dearomative annulation, PhOLED device, bond

Relation: https://figshare.com/articles/journal_contribution/Palladium-Catalyzed_Cascade_Dearomative_Spirocyclization_and_C_H_Annulation_of_Aromatic_Halides_with_Alkynes/14792112

الاتاحة: https://doi.org/10.1021/acs.orglett.1c01736.s001

المؤلفون: Shu-Shuai Chen (14259625), Xiao Tong (1560847), Xiang-Yu Liu (258990), Cheng-Yu Zheng (14259628), Jun-Su Zhou (11682313), Yao-Yue Fan (1689934), Shi-Jun He (180554), Bin Zhou (84959), Jian-Min Yue (746814)

مصطلحات موضوعية: Biochemistry, Medicine, Cell Biology, Pharmacology, Inorganic Chemistry, Space Science, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, plausible biosynthetic pathway, four highly oxygenated, >- abietane skeleton, >- abietane featuring, 6 spirocyclic scaffold, 4 , 3 , baccaurea ramiflora baccaramiones, 1 , baccaurea ramiflora, >- 15, ent <, abeo <, (< b, unique 5, trinor -<, spectroscopic analysis, rearranged trinorditerpenoids, ray crystallography, novel 20, first example

Relation: https://figshare.com/articles/journal_contribution/Baccaramiones_A_D_Four_Highly_Oxygenated_and_Rearranged_Trinorditerpenoids_from_Baccaurea_ramiflora/21727210

الاتاحة: https://doi.org/10.1021/acs.joc.2c02442.s001