+++6 Org Lett (ACS Publications) 2 Synthesis

[OrganicChemist]

Уважаемые коллеги, помогите, пожалуйста, скачать статьи:

1. Stereoselective Total Synthesis of Bioactive Marine Natural Product Biselyngbyolide B

Sayantan Das, Debobrata Paul, and Rajib Kumar Goswami

Org. Lett., Article ASAP

DOI:

Код: Выделить всё

 dx.doi.org/10.1021/acs.orglett.6b00713 

2. Synthesis of the C22–C40 Domain of the Azaspiracids

Zhigao Zhang, Yong Chen, Daniel Adu-Ampratwum, Antony Akura Okumu, Nathaniel T. Kenton, and Craig J. Forsyth

Org. Lett., Article ASAP

DOI:

Код: Выделить всё

 dx.doi.org/10.1021/acs.orglett.6b00557 

3. Enantioselective Total Synthesis of Fluvirucinin B1

Guillaume Guignard, Núria Llor, Elies Molins, Joan Bosch, and Mercedes Amat

Org. Lett., Article ASAP

DOI:

Код: Выделить всё

 dx.doi.org/10.1021/acs.orglett.6b00513 

4. Silver-Catalyzed Decarboxylative Allylation of Aliphatic Carboxylic Acids in Aqueous Solution

Lei Cui, He Chen, Chao Liu, and Chaozhong Li

Org. Lett., Article ASAP

DOI:

Код: Выделить всё

 dx.doi.org/10.1021/acs.orglett.6b00802 

5. Total Synthesis of Biselyngbyolide B

Eisuke Sato, Yurika Tanabe, Naoya Nakajima, Akifumi Ohkubo, and Kiyotake Suenaga

Org. Lett., Article ASAP

DOI:

Код: Выделить всё

 dx.doi.org/10.1021/acs.orglett.6b00660 

6. Total Synthesis of Amphirionin-4

Yusuke Ogura, Hikaru Sato, and Shigefumi Kuwahara

Org. Lett., Article ASAP

DOI:

Код: Выделить всё

 dx.doi.org/10.1021/acs.orglett.6b00883 

7. Asymmetric Synthesis of Dipropionate Derivatives through Catalytic Hydrogenation of Enantioenriched E-Ketene Heterodimers

Shi Chen, Mukulesh Mondal, Ahmad A. Ibrahim, Kraig A. Wheeler, Nessan J. Kerrigan

Synthesis, Article ASAP

DOI:

Код: Выделить всё

 dx.doi.org/10.1055/s-0035-1561958 

8. Chemoenzymatic Access to (+)-Artabotriol and its Application in Collective Synthesis of (+)-Grandiamide D, (–)-Tulipalin B, (+)-Spirathundiol, and (+)-Artabotriolcaffeate

Ramesh U. Batwal, Narshinha P. Argade

Synthesis, Article ASAP

DOI:

Код: Выделить всё

 dx.doi.org/10.1055/s-0035-1561588 

Спасибо.

[Inte]

[Inte]