Kraft Philip
Givaudan Schweiz AG, Fragrance Research, Uberlandstrasse 138, CH-8600 Dübendorf.
Chem Biodivers. 2008 Jun;5(6):970-99. doi: 10.1002/cbdv.200890108.
This review, including new experimental results, is the summary of a talk at the RSC/SCI conference 'flavours & fragrances 2007' in London, Imperial College, 24-26 September, 2007. Though the third dimension of the receptor models of J. E. Amoore rarely was exceeding 4 A, the world of woody odorants such as (+)-cedrol (3; cedarwood), (-)-khusimone (4; vetiver), and (-)-patchoulol (5; patchouli) is anything but flat. Any tricyclic skeleton with a zero-bridge contains a spirocyclic ring system determining its 3D structure, so spirocycles (spira, Lat. pretzel) are the fastest access to the third dimension. In the vetiver family, a spirocyclic mimic 9 of (-)-khusimone (4) was first discovered by chance by Büchi in 1976, and also by chance, we obtained another system, 12, with a characteristic vetiver smell by tandem-Rupe-Nazarov reaction of alkyne diols. A 5-A distance between a quaternary C-atom and a carbonyl group (or alternative HB acceptor) with an alpha-methyl or methylene branching is proposed to be the key to their vetiver odor. Upon scale-up of one of these odorants, 24, we discovered a very powerful (0.067 ng/l) impurity with a most typical patchouli scent: the spirocyclic, sterically crowded hydroxy ketone 33--a most unusual structure for a patchouli odorant. Several spirocyclic hydroxy ketone analogs, also with inverted ring systems such as in 70 and 84, provided new insights into the structure-odor correlation of this family. A superposition analysis indicated the carbonyl function of the hydroxy ketone to overlay on the geminal dimethyl motive of (-)-patchoulol. And indeed, the corresponding hydroxy ketone of patchoulol, 59, synthesized in 13 steps from Cyclal C (63), also emanated a patchouli odor. Finally, the synthesis and olfactory properties of twelve rigid spirocyclic analogs, 95-97, 99-102, and 106-110, of Georgywood (91) are presented that highlight stereochemical requirements for woody odorants and raise doubts about an alpha-helical binding motive postulated by Hong and Corey.
本综述,包括新的实验结果,是2007年9月24日至26日在伦敦帝国理工学院举行的皇家化学学会/英国化学工业协会“香料与香精2007”会议上一场报告的总结。尽管J. E. 阿莫尔受体模型的第三维度很少超过4埃,但诸如(+)-雪松醇(3;雪松木)、(-)-香根草酮(4;岩兰草)和(-)-广藿香醇(5;广藿香)等木质气味剂的世界绝非平面。任何具有零桥的三环骨架都包含一个决定其三维结构的螺环系统,因此螺环(spira,拉丁语,意为椒盐卷饼)是进入第三维度的最快途径。在岩兰草家族中,(-)-香根草酮(4)的螺环类似物9于1976年由布赫偶然首次发现,同样偶然的是,我们通过炔二醇的串联鲁佩 - 纳扎罗夫反应得到了另一个具有特征性岩兰草气味的体系12。季碳原子与具有α - 甲基或亚甲基支链的羰基(或替代的氢键受体)之间5埃的距离被认为是它们具有岩兰草气味的关键。在放大其中一种气味剂24时,我们发现了一种非常强效(0.067纳克/升)的杂质,具有最典型的广藿香香味:螺环、空间拥挤的羟基酮33——这是一种非常不寻常的广藿香气味剂结构。几种螺环羟基酮类似物,如70和84中具有倒转的环系统,为该家族的结构 - 气味相关性提供了新的见解。叠加分析表明羟基酮的羰基功能与(-)-广藿香醇的偕二甲基基团重叠。实际上,从环戊烷C(63)经13步合成的广藿香醇相应的羟基酮59也散发出广藿香气味。最后,介绍了乔治亚木(91)的十二种刚性螺环类似物95 - 97、99 - 102和106 - 110的合成及嗅觉性质,这些突出了木质气味剂的立体化学要求,并对洪和科里提出的α - 螺旋结合模式提出了质疑。