Combining enyne metathesis with long-established organic transformations: a powerful strategy for the sustainable synthesis of bioactive molecules

• Valerian Dragutan,
• Ileana Dragutan,
• Albert Demonceau and
• Lionel Delaude

Beilstein J. Org. Chem. 2020, 16, 738–755, doi:10.3762/bjoc.16.68

• in the pyrrolidine ring catalyzed by RhCl3·H2O, followed by debenzylation, amidation, and aminal generation using the Stille protocol [77]. (–)‐Clavukerin A and related sesquiterpenes Applying original organocatalytic/metal-catalyzed tactics, Metz et al. [78] reported a tandem dienyne RCM for the

• synthesis of the marine sesquiterpenoid (−)‐clavukerin A (9) and its stereoisomer (−)‐isoclavukerin A (10, Scheme 13). The sterically related analogs (+)-clavularin A and clavularin B have also been produced by this protocol. It is noteworthy, that the authors succeeded in preparing the two enantiopure

• , respectively, by domino metathesis reactions using the Hoveyda–Grubbs catalyst (4 mol %). In the final step, (−)‐clavukerin A was effectively converted into (+)-clavularin A and the latter epimerized to (−)-clavularin B. Recently, (–)-isoguaiene (11), a member of the guaiane sesquiterpenes and structurally

An efficient synthesis of the guaiane sesquiterpene (−)-isoguaiene by domino metathesis

• Yuzhou Wang,
• Ahmed F. Darweesh,
• Patrick Zimdars and
• Peter Metz

Beilstein J. Org. Chem. 2019, 15, 858–862, doi:10.3762/bjoc.15.83

• roots of Parthenium hysterophorus [5]. A recent enantioselective synthesis of (−)-isoguaiene (1) from (+)-dihydrocarvone [6] enabled an unambiguous assignment of its absolute configuration as depicted in Figure 1. Due to the structural similarity of 1 and the trisnorsesquiterpene clavukerin A (2), we

• feature a domino metathesis event and an organocatalytic Michael addition as the key steps. In closer analogy to our improved synthesis of clavukerin A (2) [8], a relay metathesis [9] of trienyne 3 was expected to lead to the hydroazulene 1 selectively. Trienyne 3 was envisioned to result from a

• sesquiterpene (−)-isoguaiene (1) using either a trienyne or a dienediyne metathesis and highly diastereoselective organocatalytic Michael additions of aldehydes derived from 5 as the key steps. Structures of the sesquiterpene (−)-isoguaiene (1) and the trisnorsesquiterpene clavukerin A (2). Retrosynthetic

A racemic formal total synthesis of clavukerin A using gold(I)-catalyzed cycloisomerization of 3-methoxy-1,6-enynes as the key strategy

• Jae Youp Cheong and
• Young Ho Rhee

Beilstein J. Org. Chem. 2011, 7, 740–743, doi:10.3762/bjoc.7.84

• Jae Youp Cheong Young Ho Rhee Department of Chemistry, POSTECH (Pohang University of Science and Technology), Hyoja-dong san 31, Nam-gu, Pohang, Kyungbook, Republic of Korea 790-784 10.3762/bjoc.7.84 Abstract An efficient formal total synthesis of (±)-clavukerin A was accomplished via a gold

• -catalyzed cycloisomerization of a 3-methoxy-1,6-enyne 5 as the key strategy followed by Rh-catalyzed stereoselective hydrogenation of the cycloheptenone 4. Keywords: clavukerin A; cycloisomerization; gold catalyst; hydrogenation; stereoselectivity; Findings Clavukerin A is a member of marine trinorguaiane

• sesquiterpene natural products. It was first isolated in 1983, by the group of Kitawara, from the Okinawa soft coral Clavularia koellikeri. The structure of clavukerin A was established by CD spectra and X-ray diffraction [1]. The first total synthesis of clavukerin A was reported by Asaoka in 1991, which was