𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Both Enantiomers of N-Boc-indoline-2-carboxylic Esters.

✍ Scribed by Masayuki Kurokawa; Takeshi Sugai

Book ID
101965608
Publisher
John Wiley and Sons
Year
2004
Weight
142 KB
Volume
35
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Structure–activity relationship of indol
Structure–activity relationship of indoline-2-carboxylic acid N-(substituted)phenylamide derivatives
✍ Jae-Hwan Kwak; Yoseob Kim; Hyunjeong Park; Jae-Yong Jang; Keun Kuk Lee; Wonhui Y 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 251 KB

Chroman derivatives exhibited potent inhibitory activity of NF-kappaB. For SAR, the chroman scaffold was modified with an indoline moiety. A series of indoline-2-carboxylic acid N-(substituted)phenylamide derivatives were synthesized to explore their inhibitory activities of NF-kappaB and they were

Chemoenzymatic Synthesis of Both Enantio
Chemoenzymatic Synthesis of Both Enantiomers of 2-tert-Butyl-2-methyl-1,3-benzodioxole-4-carboxylic (TBMB) Acid
✍ Toshinori Higashi; Chika Abe; Keiko Ninomiya; Takuya Machida; Nobuyuki Chishima; 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 281 KB 👁 2 views

## Abstract Both enantiomers of 2‐__tert__‐butyl‐2‐methyl‐1,3‐benzodioxole‐4‐carboxylic (TBMB) acid, which has a unique quaternary chiral center located on the acetal carbon, were prepared from a racemic ketone in which the carboxy group was replaced by a trifluoroacetyl group. First, reduction wit