Natural Products in OBC

Organic & Biomolecular 竞猜Chemistry,our sister journal,publishes many articles that cover a variety of natural product 竞猜chemistry.

We try to keep you updated here,although signing up toOBC'se-alert(free service) means you will receive the tables of content directly in your inbox every time an issue is published.

Hand-picked for you from the latest issues are:

Bioinspired total syntheses of terpenoids
Cedric L.Hugelshofer and Thomas Magauer
DOI: 10.1039/C6OB02488B,Perspective

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Total synthesis and confirmation of the revised structures of jiangrines A,C and D
Zhijiang Zhang and Bo Liu
DOI: 10.1039/C6OB02379G,Paper

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Fluorometabolite biosynthesis: isotopically labelled glycerol incorporations into the antibiotic nucleocidin in Streptomyces calvus
Axel Bartholomé,Jeffrey E.Janso,Usa Reilly and David O'Hagan
DOI: 10.1039/C6OB02291J,Communication

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Enantiospecific total syntheses of meroterpenoids (−)-F1839-I and (−)-corallidictyals B and D
Dattatraya H.Dethe,Balu D.Dherange,Saghir Ali and Mahesh M.Parsutkar
DOI: 10.1039/C6OB02322C,Communication

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Second-generation total synthesis of aplyronine A featuring Ni/Cr-mediated coupling reactions
Ichiro Hayakawa,Keita Saito,Sachiko Matsumoto,Shinichi Kobayashi,Ayaka Taniguchi,Kenichi Kobayashi,Yusuke Fujii,Takahiro Kaneko and Hideo Kigoshi
DOI: 10.1039/C6OB02241C,Paper

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The first total synthesis of the marine acetylenic alcohol,lembehyne B – a selective inducer of early apoptosis in leukemia cancer cells
Lilya U.Dzhemileva,Vladimir A.D'yakonov,Aleksey A.Makarov,Evgeny N.Andreev,Milyausha M.Yunusbaeva and Usein M.Dzhemilev
DOI: 10.1039/C6OB02346K,Paper

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An efficient approach to trans-4-hydroxy-5-substituted 2-pyrrolidinones through a stereoselective tandem Barbier process: divergent syntheses of (3R,4S)-statines,(+)-preussin and (−)-hapalosin
Chang-Mei Si,Lu-Ping Shao,Zhuo-Ya Mao,Wen Zhou and Bang-Guo Wei
DOI: 10.1039/C6OB02523D,Paper

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A protecting-group-free synthesis of (+)-nephrosteranic,(+)-protolichesterinic,(+)-nephrosterinic,(+)-phaseolinic,(+)-rocellaric acids and (+)-methylenolactocin
Jothi L.Nallasivam and Rodney A.Fernandes
DOI: 10.1039/C6OB02398C,Paper

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Stepwise cyclopropanation on the polycyclopropanated polyketide formation in jawsamycin biosynthesis
Tomoshige Hiratsuka,Hideaki Suzuki,Atsushi Minami and Hideaki Oikawa
DOI: 10.1039/C6OB02675C,Communication

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A novel withanolide with an unprecedented carbon skeleton from Physalis angulata
Cheng-Peng Sun,Andrei G.Kutateladze,Feng Zhao,Li-Xia Chen and Feng Qiu
DOI: 10.1039/C6OB02656G,Communication

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Total synthesis and biological activity of dolastatin 16
Loida O.Casalme,Arisa Yamauchi,Akinori Sato,Julie G.Petitbois,Yasuyuki Nogata,Erina Yoshimura,Tatsufumi Okino,Taiki Umezawa and Fuyuhiko Matsuda
DOI: 10.1039/C6OB02657E,Paper

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New compounds from a hydrothermal vent crab-associated fungus Aspergillus versicolor XZ-4
Chengqian Pan,Yutong Shi,Xuegang Chen,Chen-Tung Arthur Chen,Xinyi Tao and Bin Wu
DOI: 10.1039/C6OB02374F,Paper

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Chemoenzymatic synthesis of unmodified heparin oligosaccharides: cleavage of p-nitrophenyl glucuronide by alkaline and Smith degradation
Xing Zhang,Yongmei Xu,Po-Hung Hsieh,Jian Liu,Lei Lin,Eric P.Schmidt and Robert J.Linhardt
DOI: 10.1039/C6OB02603F,Paper

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Isoafricanol synthase from Streptomyces malaysiensis
Patrick Rabe,Markiyan Samborskyy,Peter F.Leadlay and Jeroen S.Dickschat
DOI: 10.1039/C7OB00234C,Communication

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An efficient Ugi-3CR/aza Diels–Alder/Pomeranz–Fritsch protocol towards novel aza-analogues of (±)-nuevamine,(±)-lennoxamine and magallanesine: a diversity oriented synthesis approach
Óscar Vázquez-Vera,Jorge S.Sánchez-Badillo,Alejandro Islas-Jácome,Manuel A.Rentería-Gómez,Shrikant G.Pharande,Carlos J.Cortes-García,Mónica A.Rincón-Guevara,Ilich A.Ibarra,Rocío Gámez-Montaño and Eduardo González-Zamora
DOI: 10.1039/C6OB02572B,Paper

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Intramolecular macrolactonization,photophysical and biological studies of new class of polycyclic pyrrole derivatives
Suresh Kumar Mondal,Arabinda Mandal,Susanta Kumar Manna,Sk Asraf Ali,Maidul Hossain,Vangala Venugopal,Avijit Jana and Shubhankar Samanta
DOI: 10.1039/C7OB00160F,Paper

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