Stereoselective synthesis of the diazonamide a macrocyclic core

Ilga Mutule; Beomjun Joo; Zane Medne; Toms Kalnins; Edwin Vedejs; Edgars Suna

doi:10.1021/jo5029419

Stereoselective synthesis of the diazonamide a macrocyclic core

Ilga Mutule
, Beomjun Joo
, Zane Medne
, Toms Kalnins
, Edwin Vedejs
, Edgars Suna^*

^*Šī darba korespondējošais autors

Latvian Institute of Organic Synthesis
University of Michigan, Ann Arbor

Zinātniskās darbības rezultāts: Devums žurnālam › Zinātniskais raksts (žurnālā) › koleģiāli recenzēts

18 Atsauces (Scopus)

Kopsavilkums

Stereoselective synthesis of the right-hand heteroaromatic macrocycle of diazonamide A features C16-C18 bond formation in the Suzuki-Miyaura cross-coupling and atropodiastereoselective Dieckmann-type macrocyclization as key steps. The Suzuki-Miyaura cross-coupling gave the best yields when it was catalyzed by a palladium-dioxygen complex.

Oriģinālvaloda	Angļu
Lapas (no-līdz)	3058-3066
Lapu skaits	9
Žurnāls	Journal of Organic Chemistry
Sējums	80
Izdevuma numurs	6
DOIs	https://doi.org/10.1021/jo5029419
Publikācijas statuss	Publicēts - 20 marts 2015
Ārēji publicēts	Jā

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title = "Stereoselective synthesis of the diazonamide a macrocyclic core",

abstract = "Stereoselective synthesis of the right-hand heteroaromatic macrocycle of diazonamide A features C16-C18 bond formation in the Suzuki-Miyaura cross-coupling and atropodiastereoselective Dieckmann-type macrocyclization as key steps. The Suzuki-Miyaura cross-coupling gave the best yields when it was catalyzed by a palladium-dioxygen complex.",

author = "Ilga Mutule and Beomjun Joo and Zane Medne and Toms Kalnins and Edwin Vedejs and Edgars Suna",

note = "Publisher Copyright: {\textcopyright} 2015 American Chemical Society.",

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doi = "10.1021/jo5029419",

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T1 - Stereoselective synthesis of the diazonamide a macrocyclic core

AU - Mutule, Ilga

AU - Joo, Beomjun

AU - Medne, Zane

AU - Kalnins, Toms

AU - Vedejs, Edwin

AU - Suna, Edgars

PY - 2015/3/20

Y1 - 2015/3/20

N2 - Stereoselective synthesis of the right-hand heteroaromatic macrocycle of diazonamide A features C16-C18 bond formation in the Suzuki-Miyaura cross-coupling and atropodiastereoselective Dieckmann-type macrocyclization as key steps. The Suzuki-Miyaura cross-coupling gave the best yields when it was catalyzed by a palladium-dioxygen complex.

AB - Stereoselective synthesis of the right-hand heteroaromatic macrocycle of diazonamide A features C16-C18 bond formation in the Suzuki-Miyaura cross-coupling and atropodiastereoselective Dieckmann-type macrocyclization as key steps. The Suzuki-Miyaura cross-coupling gave the best yields when it was catalyzed by a palladium-dioxygen complex.

UR - https://www.scopus.com/pages/publications/84925352869

U2 - 10.1021/jo5029419

DO - 10.1021/jo5029419

M3 - Article

C2 - 25705925

AN - SCOPUS:84925352869

SN - 0022-3263

VL - 80

SP - 3058

EP - 3066

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 6

ER -

Stereoselective synthesis of the diazonamide a macrocyclic core

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