An enantioselective synthesis of (+)-pseudohygroline.

• The enantioselective synthesis of (+)-pseudohygroline (3), employing a highly diastereoselective ring closure as a key step, has been achieved in seven steps from readily available protected lactaldehyde (6). (C) 1998 Elsevier Science Ltd. All rights res

Keyword

INTRAMOLECULAR OXYMERCURATIONS

Publication and Content Type

vet (subject category)

ovr (subject category)