(4R,6R,7R,8S,10S)-9-hydroxy-6,7-(isopropylidenedioxy)-4,6,8,10-tetramethyldodec-11-en-3-one | 123074-54-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (4R,6R,7R,8S,10S)-9-hydroxy-6,7-(isopropylidenedioxy)-4,6,8,10-tetramethyldodec-11-en-3-one
• 英文别名: (2R)-1-[(4R,5R)-5-[(2S,3R,4S)-3-hydroxy-4-methylhex-5-en-2-yl]-2,2,4-trimethyl-1,3-dioxolan-4-yl]-2-methylpentan-3-one
• CAS: 123074-54-4
• 化学式: C₁₉H₃₄O₄
• 分子量: 326.477
• InChiKey: WFWDMXJSJIAOTP-RTEVUOIBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  23
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.84
• 拓扑面积：
  55.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (4R,6R,7R,8S,10S)-9-hydroxy-6,7-(isopropylidenedioxy)-4,6,8,10-tetramethyldodec-11-en-3-one 在 oil scarlet 、 臭氧 、 三乙胺 、 lithium hexamethyldisilazane 作用下， 反应 3.75h， 生成 (2R,3S,4S)-4-[(4R,5R)-5-((2R,4R,5S,6R)-7-Benzyloxymethoxy-5-hydroxy-2,4,6-trimethyl-3-oxo-nonyl)-2,2,5-trimethyl-[1,3]dioxolan-4-yl]-3-hydroxy-2-methyl-pentanoic acid methyl ester
  参考文献：
  名称：

  erythronolide B的seco-酸的简明不对称合成

  摘要：

  3，一种被保护的赤藓酮内酯 B 的二烯酸衍生物，通过收敛方法实现，其中最长的线性序列仅使用 14 个化学操作，总步数为 18。该方法有效且实质性可以准备大量的材料

  DOI：

  10.1021/ja00201a066
• 作为产物：
  描述：

  (2S,3R,4R,6R)-7,7-(ethylenedithio)-3,4-(isopropylidenedioxy)-2,4,6-trimethylnonanol 在 N-溴代丁二酰亚胺(NBS) 、 草酰氯 、 三氟化硼乙醚 、 二甲基亚砜 、 三乙胺 作用下， 以 二氯甲烷 、 水 、 丙酮 为溶剂， 反应 1.25h， 生成 (4R,6R,7R,8S,10S)-9-hydroxy-6,7-(isopropylidenedioxy)-4,6,8,10-tetramethyldodec-11-en-3-one
  参考文献：
  名称：

  erythronolide B的seco-酸的简明不对称合成

  摘要：

  3，一种被保护的赤藓酮内酯 B 的二烯酸衍生物，通过收敛方法实现，其中最长的线性序列仅使用 14 个化学操作，总步数为 18。该方法有效且实质性可以准备大量的材料

  DOI：

  10.1021/ja00201a066

文献信息

• Effect of metal counterions on the stereoselectivity of aldol reactions used to assemble the seco acid backbone of erythromycin b
  作者：Stephen F. Martin、Wen-Cherng Lee

  DOI：10.1016/s0040-4039(00)73542-8

  日期：1993.4

  reactions of the enolates derived from the ketones 11, 15, and 19 with the aldehyde 2a depended upon whether the counterion was lithium or titanium. For lithium enolates the stereoselectivity appeared to be controlled by the stereochemistry alpha to the carbonyl group of the aldehyde partner, whereas the stereochemistry at the α′-carbon of the enolate was important for the titanium enolate.

  从酮衍生的烯醇化物的醛醇缩合反应的选择性diastereofacial 11，15，和19与醛2A依赖于抗衡离子是否锂或钛。对于烯醇锂而言，立体选择性似乎受α-醛配体的羰基的立体化学控制，而烯醇钛的α'-碳上的立体化学对于烯醇钛是重要的。
• Strategies for Macrolide Synthesis. A Concise Approach to Protected Seco-Acids of Erythronolides A and B
  作者：Stephen F. Martin、Wen-Cherng Lee、Gregory J. Pacofsky、Ricky P. Gist、Thomas A. Mulhern

  DOI：10.1021/ja00090a016

  日期：1994.6

  Concise syntheses of protected derivatives of the seco-acids of erythronolides A and B, 5 and 6, respectively, have been completed wherein the longest linear sequence requires only 13 chemical steps from 5-ethylfuraldehyde (15). The syntheses commenced with the asymmetric aldol condensation of 15 according to the Evans protocol to afford the optically pure syn adduct 16, thereby establishing the critical stereocenters at C(4) and C(5) of the erythromycin backbone. Reductive removal of the chiral auxiliary from 16 gave the diol 17, which was converted to the bicyclic enone 18 by an one-pot process involving sequential oxidation of the furan ring and acid-catalyzed bicycloketalization. Stereoselective elaboration of 18 to the tertiary alcohol 19 was achieved in two steps by sequential treatment with lithium dimethylcuprate and methyllithium in the presence of cerium trichloride. Compound 19 underwent facile acid-catalyzed reorganization to the isomeric ketal 21, which was transformed into 24 by a Swern oxidation and a second asymmetric aldol condensation. However, the necessary refunctionalization of 24 into a ketone that would participate in the requisite aldol reaction to append the C(11)-C(15) segment of the erythronolide backbone could not be induced. On the other hand, transthioketalization of 19 gave the triol 26, which was converted to 28 by the thermodynamically-controlled formation of an acetonide of the 1,2-diol array. Deprotection of the C(9) ketone function followed by Swern oxidation produced the keto aldehyde 31, which underwent chemoselective, Lewis acid-mediated addition of tri-n-butylcrotylstannane to the aldehyde function to furnish a mixture (4:1) of the homoallylic alcohols 32 and 33; the major product 32 comprises the C(1)-C(10) subunit common to the seco-acids of both erythronolides A and B. Diastereoselective aldol condensation of the enolate derived from 32 with 40 gave 42 as the major adduct; oxidative processing of the terminal olefin then delivered the erythronolide B seco-acid derivative 46. The proposed structure of 42 was initially based upon its conversion into the polyol 48, which was identical to that derived from natural erythronolide B (49). Subsequent to this chemical correlation, the X-ray structure of 50, which was prepared from 42, unequivocally verified this assignment. In experiments directed toward the preparation of the seco-acid of erythronolide A, the directed aldol reactions of 32 with the aldehydes 59 and 60 were examined. Although the addition of the enolate of 32 to 59 produced none of the requisite adduct, its reaction with 60 gave a mixture (1:5) of 62 and 64. Stereoselective reduction of the C(9) carbonyl function of 62 followed by oxidative cleavage of the double bond and global deprotection gave the polyol 62, which was identical with the polyol derived from natural erythromycin A (1).
• A concise asymmetric synthesis of the seco-acid of erythronolide B
  作者：Stephen F. Martin、Gregory J. Pacofsky、Ricky P. Gist、Wen Cherng Lee

  DOI：10.1021/ja00201a066

  日期：1989.9

  The concise synthesis of 3,a protected derivative of the seco acid of erythronolide B, has been achieved by a convergent approach wherein the longest linear sequence employs only 14 chemical operations with the total number of steps being 18. The approach is efficient, and substantial quantities of material may be prepared

  3，一种被保护的赤藓酮内酯 B 的二烯酸衍生物，通过收敛方法实现，其中最长的线性序列仅使用 14 个化学操作，总步数为 18。该方法有效且实质性可以准备大量的材料