Your browser doesn't support javascript.
loading
Chemzymes: a new class of structurally rigid tricyclic amphibian organocatalyst inspired by natural product.
Xiao, Jian; Xu, Feng-Xia; Lu, Yun-Peng; Loh, Teck-Peng.
Affiliation
  • Xiao J; Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371.
Org Lett ; 12(6): 1220-3, 2010 Mar 19.
Article in En | MEDLINE | ID: mdl-20158252
ABSTRACT
A new class of structurally rigid tricyclic amphibian chiral catalyst was rationally designed based on the hexahydropyrrolo[2,3-b]indole skeleton as a new type of chemzyme. This new type of chemzyme possesses a structurally rigid tricyclic skeleton and a chiral pocket which provides a well-organized chiral environment for asymmetric induction, as well as a hydrophobic pocket to enable organocatalytic reactions to proceed smoothly both in organic solvents and in water.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyrroles / Biological Products / Drug Design / Indoles Limits: Animals Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2010 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyrroles / Biological Products / Drug Design / Indoles Limits: Animals Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2010 Document type: Article