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1.
Org Lett ; 24(32): 5924-5928, 2022 Aug 19.
Article in English | MEDLINE | ID: mdl-35930708

ABSTRACT

A novel and efficient copper-catalyzed transannular ring-closing reaction of eight-membered rings has been developed that provides a straightforward way to synthesize bicyclo[3.3.0]octane derivatives in good yields. Mechanistic studies revealed that the reaction pathway might involve chlorination followed by the Kornblum reaction. Readily accessible starting materials and good functional group tolerance make this procedure attractive.

2.
J Org Chem ; 86(9): 6755-6764, 2021 May 07.
Article in English | MEDLINE | ID: mdl-33847128

ABSTRACT

An atom economic procedure for the regioselective synthesis of bridged seven-membered-ring compounds from simple reactants such as ynones and indene-1,3-dione has been developed. This process was realized through the one-pot reactions of ring-expansion of indene-1,3-dione with alkynyl ketones and successive formal [4+2] cycloaddition. The Michael addition reaction is the key for the regioselectivity of the formal [4+2] cycloaddition.

3.
Org Biomol Chem ; 18(35): 6916-6926, 2020 09 21.
Article in English | MEDLINE | ID: mdl-32869825

ABSTRACT

A cascade reaction involving the Zn-catalyzed dearomatization of indoles, base-promoted ring-expansion and intramolecular SNAr reaction has been developed. This process realized a novel, atom economical and efficient synthesis of indoline-fused eight-membered azaheterocycles in a one pot manner.

4.
Org Lett ; 22(16): 6532-6536, 2020 08 21.
Article in English | MEDLINE | ID: mdl-32806175

ABSTRACT

A novel and efficient synthesis of aza-eight-membered ring-fused indolines has been developed. This process is realized by zinc-catalyzed C2 alkylation of indoles and subsequent base-promoted ring expansion of the newly formed six-membered ring with alkynes. Easily accessible starting materials, good functional group tolerance, and high atom economy make this procedure attractive.

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