Highly Enantioselective Formal Synthesis of (+)‐Treprostinil Enabled by Rhodium‐Catalyzed Enyne Cycloisomerization DOI
Yan Zong, Shuang Gao,

Xiaomei Zou

и другие.

Chinese Journal of Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Апрель 30, 2025

Comprehensive Summary Herein, a highly enantioselective formal synthesis of (+)‐Treprostinil via the interphenylene prostaglandin E 1 scaffold was described. The chiral multi‐substituted cyclopentanone constructed [Rh(Duanphos)SbF 6 ‐catalyzed asymmetric enyne cycloisomerization and copper hydride‐mediated conjugate reduction. In addition, new type obtained Alder‐ene reaction in high yield with excellent chemoselectivity.

Язык: Английский

Highly Enantioselective Formal Synthesis of (+)‐Treprostinil Enabled by Rhodium‐Catalyzed Enyne Cycloisomerization DOI
Yan Zong, Shuang Gao,

Xiaomei Zou

и другие.

Chinese Journal of Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Апрель 30, 2025

Comprehensive Summary Herein, a highly enantioselective formal synthesis of (+)‐Treprostinil via the interphenylene prostaglandin E 1 scaffold was described. The chiral multi‐substituted cyclopentanone constructed [Rh(Duanphos)SbF 6 ‐catalyzed asymmetric enyne cycloisomerization and copper hydride‐mediated conjugate reduction. In addition, new type obtained Alder‐ene reaction in high yield with excellent chemoselectivity.

Язык: Английский

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