Journal
CHEMICAL COMMUNICATIONS
Volume 47, Issue 38, Pages 10821-10823Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c1cc13992d
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Funding
- EPSRC
- GSK
- University of Medicine and Pharmacy
- Ho Chi Minh City
- University of Manchester
- Engineering and Physical Sciences Research Council [EP/G015287/1] Funding Source: researchfish
- EPSRC [EP/G015287/1] Funding Source: UKRI
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A connective Pummerer-type cyclisation involving a cysteine derivative and an N-benzyl glyoxamide 3 has been applied in an asymmetric synthesis of the protected ABH rings 2 of the antitumour and antimicrobial natural product ecteinascidin 597.
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