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1.
J Org Chem ; 84(15): 9561-9569, 2019 08 02.
Article in English | MEDLINE | ID: mdl-31257884

ABSTRACT

Rh(II)-catalyzed reactions of 3-diazoindolin-2-imines with 3-(2-bromoethyl)indoles, 3-(3-bromopropyl)indoles, and 3-(4-bromobutyl)indoles, followed by treatment with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in a one-pot operation furnished azepino[2,3-b:4,5-b']diindoles, azocino[2,3-b:4,5-b']diindoles, and azonino[2,3-b:4,5-b']diindoles, respectively. Structural uniqueness of the products, broad substrate scope, mild reaction conditions, and readily available starting materials are the merits of this approach.

2.
Chem Commun (Camb) ; 54(12): 1529-1532, 2018 Feb 11.
Article in English | MEDLINE | ID: mdl-29367964

ABSTRACT

3-Diazoindolin-2-imines reacted with chiral 2-(phenylamino)ethanols under copper catalysis to furnish chiral spiro[indoline-3,2'-oxazolidin]-2-imines in good yields with excellent diastereoselectivity. The reaction undergoes a copper-catalyzed cascade process involving the formation of copper carbene, C-N coupling, and C-O coupling.

3.
Org Lett ; 19(15): 4114-4117, 2017 08 04.
Article in English | MEDLINE | ID: mdl-28726422

ABSTRACT

Trifluoroboron-promoted cascade reactions between tryptophols and propagylic alcohols furnished three types of skeletons, including carbazoles, cyclopenta[b]furo[2,3-b]indoles, and allenyl furo[2,3-b]indoles, with excellent selectivity based on the substrate structure. Tryptophols without a substituent on the 2-position of the indole ring reacted with 1,1,3-triphenylprop-2-yn-1-ol and 9-(phenylethynyl)-9H-fluoren-9-ol to give carbazoles and cyclopenta[b]furo[2,3-b]indoles, respectively, while the reaction of 2-substituted tryptophols afforded allenylfuro[2,3-b]indoles.

4.
J Org Chem ; 82(10): 5294-5300, 2017 05 19.
Article in English | MEDLINE | ID: mdl-28474887

ABSTRACT

An efficient and highly regioselective synthesis of 1-allenyl-5-aryl-1,2,3-triazoles from 1-sulfonyl-4-aryl-1,2,3-triazoles is disclosed. 1-Sulfonyl-4-aryl-1,2,3-triazoles reacted with propargylic alcohols in the presence of trifluoroboron etherate to furnish 1-allenyl-5-aryl-1,2,3-triazoles. When secondary alcohols were used as substrate, the outcome of the reaction was 1-alkyl-5-aryl-1,2,3-triazoles.

5.
Org Lett ; 18(15): 3682-5, 2016 08 05.
Article in English | MEDLINE | ID: mdl-27391393

ABSTRACT

Rhodium-catalyzed reactions of 3-diazoindolin-2-imines with aromatic aldehydes and α,ß-unsaturated aldehydes respectively furnished (E)-2-aminomethylene-3-oxoindoles and pyranoindoles in moderate to excellent yields with nice functional group tolerance. The reaction proceeds in a cascade involving α-amidino rhodium carbene as the key intermediate.

6.
Chem Commun (Camb) ; 51(55): 11056-9, 2015 Jul 14.
Article in English | MEDLINE | ID: mdl-26068061

ABSTRACT

The rhodium-catalyzed reactions of 3-diazoindolin-2-imines with N,N-dialkylanilines, N-allyl-N-alkylanilines, and N-propargyl-N-alkylanilines and 3-diazoindolin-2-imines furnished 3-aryl-2-aminoindoles, 3-allyl-3-amino-2-iminoindolines, and tetrahydro-[1,4]diazepino[2,3-b]indoles, respectively. 3-Diazoindolin-2-imines acted as precursors of α-imino rhodium carbenes in these transformations.


Subject(s)
Imines/chemistry , Indoles/chemical synthesis , Catalysis , Indoles/chemistry , Molecular Structure , Organometallic Compounds/chemistry , Rhodium/chemistry
7.
Org Lett ; 16(19): 5096-9, 2014 Oct 03.
Article in English | MEDLINE | ID: mdl-25211289

ABSTRACT

3-Diazoindolin-2-imines were constructed from indoles and sulfonylazides via an electronically matched 1,3-dipolar cycloaddition and a subsequent dehydroaromatization/ring-opening cascade. The reaction between 3-substituted indoles and sulfonyl azides provided 2-aminoindoles, while 2-substituted indoles furnished 3-aminoindoles. Moreover, 2,3-diaminoindoles could be prepared from the resulting 3-diazoindolin-2-imines and secondary amines via a rhodium-catalyzed amination. Further extension of 2,3-diaminoindoles led to the formation of imidazo[4,5-b]indoles.


Subject(s)
Azides/chemistry , Heterocyclic Compounds, 3-Ring/chemical synthesis , Imidazoles/chemical synthesis , Imines/chemical synthesis , Indoles/chemical synthesis , Amination , Amines/chemistry , Catalysis , Cycloaddition Reaction , Heterocyclic Compounds, 3-Ring/chemistry , Imidazoles/chemistry , Imines/chemistry , Indoles/chemistry , Molecular Structure , Rhodium/chemistry
8.
Org Lett ; 16(4): 1244-7, 2014 Feb 21.
Article in English | MEDLINE | ID: mdl-24517549

ABSTRACT

3-Sulfonyl[1,2,3]triazolo[4,5-b]indoles were efficiently prepared via a tandem catalysis process involving intramolecular ligand stabilized CuAAC and Cu-catalyzed C-N coupling. The obtained 3-sulfonyl[1,2,3]triazolo[4,5-b]indoles could be utilized as α-imino rhodium carbene precursors for the construction of a range of valuable indole molecules including pyrrolo[2,3-b]indoles, spirocyclopropyl iminoindoles, 2,3-dihydropyrrolo[2,3-b]indoles, 3,3'-biindoles, and 2,3'-biindoles.


Subject(s)
Copper/chemistry , Indoles/chemical synthesis , Rhodium/chemistry , Sulfones/chemical synthesis , Triazoles/chemical synthesis , Catalysis , Indoles/chemistry , Methane/analogs & derivatives , Methane/chemistry , Molecular Structure , Stereoisomerism , Sulfones/chemistry , Triazoles/chemistry
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