Jiang, B. et al. published their research in Tetrahedron Letters in 2001 | CAS: 149108-61-2

(1-tosyl-1H-Indol-3-yl)boronic acid (cas: 149108-61-2) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. In addition to indole, the strain-release chemistry worked for numerous substrates including amines, alcohols, thiols, carboxylic acids, imidazoles, and pyrazoles.Formula: C15H14BNO4S

A highly stereoselective synthesis of indolyl N-substituted glycines was written by Jiang, B.;Yang, C.-G.;Gu, X.-H.. And the article was included in Tetrahedron Letters in 2001.Formula: C15H14BNO4S This article mentions the following:

Optically active N-substituted 伪-indolylglycines were synthesized with high diastereoselectivity by Mannich reaction of an indolylboronic acid with glyoxylic acid using (R)-伪-methylbenzylamine as the chiral auxiliary. The absolute configuration of one of the products was determined by a single-crystal x-ray anal. In the experiment, the researchers used many compounds, for example, (1-tosyl-1H-Indol-3-yl)boronic acid (cas: 149108-61-2Formula: C15H14BNO4S).

(1-tosyl-1H-Indol-3-yl)boronic acid (cas: 149108-61-2) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. In addition to indole, the strain-release chemistry worked for numerous substrates including amines, alcohols, thiols, carboxylic acids, imidazoles, and pyrazoles.Formula: C15H14BNO4S

Referemce:
Indole alkaloid derivatives as building blocks of natural products from聽Bacillus thuringiensis聽and聽Bacillus velezensis聽and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Jiang, B. et al. published their research in Tetrahedron Letters in 2001 | CAS: 149108-61-2

(1-tosyl-1H-Indol-3-yl)boronic acid (cas: 149108-61-2) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. In addition to indole, the strain-release chemistry worked for numerous substrates including amines, alcohols, thiols, carboxylic acids, imidazoles, and pyrazoles.Formula: C15H14BNO4S

A highly stereoselective synthesis of indolyl N-substituted glycines was written by Jiang, B.;Yang, C.-G.;Gu, X.-H.. And the article was included in Tetrahedron Letters in 2001.Formula: C15H14BNO4S This article mentions the following:

Optically active N-substituted α-indolylglycines were synthesized with high diastereoselectivity by Mannich reaction of an indolylboronic acid with glyoxylic acid using (R)-α-methylbenzylamine as the chiral auxiliary. The absolute configuration of one of the products was determined by a single-crystal x-ray anal. In the experiment, the researchers used many compounds, for example, (1-tosyl-1H-Indol-3-yl)boronic acid (cas: 149108-61-2Formula: C15H14BNO4S).

(1-tosyl-1H-Indol-3-yl)boronic acid (cas: 149108-61-2) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. In addition to indole, the strain-release chemistry worked for numerous substrates including amines, alcohols, thiols, carboxylic acids, imidazoles, and pyrazoles.Formula: C15H14BNO4S

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Jiang, B. et al. published their research in Tetrahedron Letters in 2001 | CAS: 149108-61-2

(1-tosyl-1H-Indol-3-yl)boronic acid (cas: 149108-61-2) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. In addition to indole, the strain-release chemistry worked for numerous substrates including amines, alcohols, thiols, carboxylic acids, imidazoles, and pyrazoles.Formula: C15H14BNO4S

A highly stereoselective synthesis of indolyl N-substituted glycines was written by Jiang, B.;Yang, C.-G.;Gu, X.-H.. And the article was included in Tetrahedron Letters in 2001.Formula: C15H14BNO4S This article mentions the following:

Optically active N-substituted α-indolylglycines were synthesized with high diastereoselectivity by Mannich reaction of an indolylboronic acid with glyoxylic acid using (R)-α-methylbenzylamine as the chiral auxiliary. The absolute configuration of one of the products was determined by a single-crystal x-ray anal. In the experiment, the researchers used many compounds, for example, (1-tosyl-1H-Indol-3-yl)boronic acid (cas: 149108-61-2Formula: C15H14BNO4S).

(1-tosyl-1H-Indol-3-yl)boronic acid (cas: 149108-61-2) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. In addition to indole, the strain-release chemistry worked for numerous substrates including amines, alcohols, thiols, carboxylic acids, imidazoles, and pyrazoles.Formula: C15H14BNO4S

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Jiang, B. et al. published their research in Tetrahedron Letters in 2001 | CAS: 149108-61-2

(1-tosyl-1H-Indol-3-yl)boronic acid (cas: 149108-61-2) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. In addition to indole, the strain-release chemistry worked for numerous substrates including amines, alcohols, thiols, carboxylic acids, imidazoles, and pyrazoles.Formula: C15H14BNO4S

A highly stereoselective synthesis of indolyl N-substituted glycines was written by Jiang, B.;Yang, C.-G.;Gu, X.-H.. And the article was included in Tetrahedron Letters in 2001.Formula: C15H14BNO4S This article mentions the following:

Optically active N-substituted α-indolylglycines were synthesized with high diastereoselectivity by Mannich reaction of an indolylboronic acid with glyoxylic acid using (R)-α-methylbenzylamine as the chiral auxiliary. The absolute configuration of one of the products was determined by a single-crystal x-ray anal. In the experiment, the researchers used many compounds, for example, (1-tosyl-1H-Indol-3-yl)boronic acid (cas: 149108-61-2Formula: C15H14BNO4S).

(1-tosyl-1H-Indol-3-yl)boronic acid (cas: 149108-61-2) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. In addition to indole, the strain-release chemistry worked for numerous substrates including amines, alcohols, thiols, carboxylic acids, imidazoles, and pyrazoles.Formula: C15H14BNO4S

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles