New frontiers in multicomponent mechanosynthesis for organic molecules: modern marvels DOI

Hiren R. Chaudhary,

Divyang M. Patel

Molecular Diversity, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 1, 2024

Language: Английский

Synthesis of Benzo[e][1,4,3]oxathiazin-3-one 1-Oxides from NH-S-(2-Hydroxyaryl)sulfoximines DOI

Kiruthika Periasamy,

Pit van Bonn,

Runa Tschekorsky Orloff

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(11), P. 8286 - 8290

Published: May 14, 2024

Cyclizations of NH-S-(2-hydroxyaryl)sulfoximines with 1,1′-carbonyldiimidazol (CDI) give unprecedented benzo[e][1,4,3]oxathiazin-3-one 1-oxides in good yields. The standard synthetic protocol involves the use DCE at an increased temperature for 16 h. Under mechanochemical conditions, a representative product was obtained without solvent ambient only 60 min. X-ray single-crystal structure analysis confirmed molecular scaffold representing three-dimensional heterocycle.

Language: Английский

Citations

1

Expedient (3+3)-annulation of carbonyl ylides with azaoxyallyl cations: formal access to oxa-benzo[c]azepin-3-ones DOI
Kshitiz Verma, Hemanga Bhattacharyya, Sharajit Saha

et al.

Chemical Communications, Journal Year: 2024, Volume and Issue: unknown

Published: Jan. 1, 2024

Cascade C–C/C–N bond formation of carbonyl ylides with azaoxyallyl cations generated in situ using Rh-catalysis has been accomplished the presence a base at room temperature.

Language: Английский

Citations

1

Access to syn α‐Amino‐β‐Hydroxyesters by N‐H Insertion on O‐Protected α‐Diazo‐β‐Hydroxyesters. DOI Creative Commons

Thomas Defuentes,

Jérôme Lhoste, Catherine Gaulon‐Nourry

et al.

Asian Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 13, 2024

Abstract The N−H insertion reaction is a versatile method for creating C−N bonds under mild conditions, providing in particular an efficient access to both natural and non‐natural α‐amino acid derivatives. In this field, the direct on α‐diazo‐β‐hydroxyesters has not yet been investigated constitutes significant challenge, due competitive migration processes. We report herein first insertions O ‐protected α‐diazo‐β‐aryl‐β‐hydroxyesters, enabling synthesize wide range of α‐amino‐β‐hydroxyesters by tuning nature amine aryl substituent. Overall, 28 products have isolated, with moderate good yields most cases, diastereoisomeric ratios up 8.0 : 1 favor syn diastereoisomer.

Language: Английский

Citations

0

New frontiers in multicomponent mechanosynthesis for organic molecules: modern marvels DOI

Hiren R. Chaudhary,

Divyang M. Patel

Molecular Diversity, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 1, 2024

Language: Английский

Citations

0