Cyclic natural product oligomers: diversity and (bio)synthesis of macrocycles

Songya Zhang, Shuai Fan, Haocheng He, Jing Zhu, Lauren Murray, Gong Liang, Shi Ran, Yi Zhun Zhu, Max J. Cryle, Hai-Yan He and Youming Zhang

Chem. Soc. Rev., 2025, 54, 396
DOI: 10.1039/D2CS00909A

Total syntheses of pamamycin 607 and methyl nonactate: stereoselective cyclisation of homoallylic alcohols that had been prepared with remote stereocontrol using allylstannanes

Olivier Germay, Naresh Kumar, Christopher G. Moore and Eric J. Thomas

Org. Biomol. Chem., 2012, 10, 9709
DOI: 10.1039/c2ob26801a

The structures of four new pamamycin homologues isolated from streptomyces alboniger

Masahiro Natsume, Kazuhisa Yasui, Satoru Kondo and Shingo Marumo

Tetrahedron Letters, 1991, 32, 3087
DOI: 10.1016/0040-4039(91)80696-4

Total Synthesis of (+)-Pamamycin-607

Sung Ho Kang, Joon Won Jeong, Yu Sang Hwang and Sung Bae Lee

Angewandte Chemie International Edition, 2002, 41, 1392
DOI: 10.1002/1521-3773(20020415)41:8<1392::AID-ANIE1392>3.0.CO;2-G

Enantioselective synthesis of the larger fragment of pamamycin-607

Heiko Bernsmann, Margit Gruner and Peter Metz

Tetrahedron Letters, 2000, 41, 7629
DOI: 10.1016/S0040-4039(00)01308-3

A shortcut to the smaller fragment of pamamycin-607

Heiko Bernsmann, Margit Gruner, Roland Fröhlich and Peter Metz

Tetrahedron Letters, 2001, 42, 5377
DOI: 10.1016/S0040-4039(01)01044-9

Total synthesis of pamamycin 607: applications of remote asymmetric induction in organic synthesis

Olivier Germay, Naresh Kumar and Eric J Thomas

Tetrahedron Letters, 2001, 42, 4969
DOI: 10.1016/S0040-4039(01)00921-2

Total synthesis of pamamycin-607

Yuzhou Wang, Heiko Bernsmann, Margit Gruner and Peter Metz

Tetrahedron Letters, 2001, 42, 7801
DOI: 10.1016/S0040-4039(01)01665-3

Synthesis of Southern (C1'-C11') and Eastern (C8-C18) Fragments of Pamamycin-607, an Aerial Mycelium-inducing Substance of Streptomyces alboniger

Hiromasa KIYOTA, Yukito FURUYA, Shigefumi KUWAHARA and Takayuki ORITANI

Bioscience, Biotechnology, and Biochemistry, 2001, 65, 2630
DOI: 10.1271/bbb.65.2630

Structure-activity Relationship of Pamamycins: Effect of Side Chain Length on Aerial Mycelium-inducing Activity

Ikuko Kozone, Makoto Hashimoto, Udo Gräfe, Hiroshi Kawaide, Hiroshi Abe and Masahiro Natsume

J Antibiot, 2008, 61, 98
DOI: 10.1038/ja.2008.118

A novel and efficient stereoselective synthesis of the southern part of pamamycin-607

Gérard Mandville, Christian Girard and Robert Bloch

Tetrahedron: Asymmetry, 1997, 8, 3665
DOI: 10.1016/S0957-4166(97)00475-8

Synthetic studies on development of a novel macrolide ionophore: Configurational requirement of 16-membered macrodiolide for binding ability

Kazushige Fujii, Osamu Hara, Shingo Marumo and Youji Sakagami

Bioorganic & Medicinal Chemistry Letters, 1995, 5, 843
DOI: 10.1016/0960-894X(95)00125-D

Antimycobacterial activity of synthetic pamamycins

P. Lefèvre, P. Peirs, M. Braibant, M. Fauville-Dufaux, R. Vanhoof, K. Huygen, X.-M. Wang, B. Pogell, Y. Wang, P. Fischer, P. Metz and J. Content

Journal of Antimicrobial Chemotherapy, 2004, 54, 824
DOI: 10.1093/jac/dkh402

An Aldol Approach to the Total Synthesis of Pamamycin 621 A

Guo-Bao Ren and Yikang Wu

Org. Lett., 2009, 11, 5638
DOI: 10.1021/ol902290v

Stereoselective synthesis of tetrahydrofurans using intramolecular oxymercurations

Agatha Garavelas, Irene Mavropoulos, Patrick Perlmutter and Gunnar Westman

Tetrahedron Letters, 1995, 36, 463
DOI: 10.1016/0040-4039(94)02287-L

Study on bioactive natural products involved in the growth and morphological differentiation of microorganisms

Masahiro Natsume

Jpn. J. Pestic. Sci., 2016, 41, 169
DOI: 10.1584/jpestics.W16-11

Toward the synthesis of pamamycin-607

Heiko Bernsmann, Benno Hungerhoff, Regina Fechner, Roland Fröhlich and Peter Metz

Tetrahedron Letters, 2000, 41, 1721
DOI: 10.1016/S0040-4039(00)00022-8

A stereocontrolled synthetic route to the C1C18 subunit of pamamycin-607

Sung Ho Kang and Joon Won Jeong

Tetrahedron Letters, 2002, 43, 3613
DOI: 10.1016/S0040-4039(02)00655-X

Four New Derivatives of Trihomononactic Acids from Streptomyces globisporus

Tomáš Řezanka, Jaroslav Spížek, Věra Přikrylová and Valery M. Dembitsky

Eur J Org Chem, 2004, 2004, 4239
DOI: 10.1002/ejoc.200400276

Total Synthesis of Oxacyclic Macrodiolide Natural Products

Eun Joo Kang and Eun Lee

Chem. Rev., 2005, 105, 4348
DOI: 10.1021/cr040629a

An Enantioselective Convergent Route to Pamamycin 621A

Guo-Bao Ren, Yi-Xian Huang, Ya-Ping Sun, Zhong-Han Li and Yikang Wu

J. Org. Chem., 2010, 75, 5048
DOI: 10.1021/jo100774n

Superior production of heavy pamamycin derivatives using a bkdR deletion mutant of Streptomyces albus J1074/R2

Lars Gläser, Martin Kuhl, Julian Stegmüller, Christian Rückert, Maksym Myronovskyi, Jörn Kalinowski, Andriy Luzhetskyy and Christoph Wittmann

Microb Cell Fact, 2021, 20
DOI: 10.1186/s12934-021-01602-6

Studies on bioactive natural products involved in the growth and morphological differentiation of microorganisms

Masahiro Natsume

Journal of Pesticide Science, 2016, 41, 96
DOI: 10.1584/jpestics.J16-03